GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **2401 - 2425** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
2619	growth arrest specific 1	GAS1	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Kallmann syndrome Laron syndrome Marfan syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Potter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia allergic asthma asthma bilateral renal aplasia bladder carcinoma bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cavernous hemangioma central nervous system cancer childhood osteosarcoma choanal atresia chorioangioma chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate collecting duct carcinoma coloboma colorectal cancer colorectal carcinoma congenital hypothyroidism degenerative disc disease diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenal atresia embryoma epilepsy gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor hemangioma hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy hermaphroditism high grade glioma histiocytoid hemangioma holoprosencephaly 1 holoprosencephaly hypertropia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism intellectual disability intramuscular hemangioma intrinsic asthma isolated cleft palate isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency kidney disease large intestine cancer learning disability lymphangioma mechanical strabismus melanoma microcephaly mixed glioma myxedema nephritis nephrosis neuroblastoma neuropathy nevoid basal cell carcinoma syndrome nonpapillary renal cell carcinoma ophthalmoplegia orofaciodigital syndrome I orofaciodigital syndrome X osteosarcoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease placental insufficiency primary open angle glaucoma pseudohermaphroditism pyoureter rabies renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy situs inversus skin melanoma solitary median maxillary central incisor stomach cancer stomach carcinoma strabismus tetralogy of Fallot thymus gland disease thyroid gland papillary carcinoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer visual epilepsy
2998	glycogen synthase 2	GYS2	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Gerstmann-Straussler-Scheinker syndrome Goldenhar syndrome Gorham's disease Joubert syndrome 1 Joubert syndrome Lafora disease Laron syndrome Moebius syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia adult medulloblastoma branchiootic syndrome cancer childhood medulloblastoma cystinuria disease of metabolism epilepsy familial hyperlipidemia galactosemia gestational diabetes glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis B hepatocellular carcinoma hyperglycemia hypoglycemia liver cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma orofaciodigital syndrome I orofaciodigital syndrome X orofaciodigital syndrome polycystic ovary syndrome visual epilepsy
4047	lanosterol synthase	LSS Aliases: OSC Oxidosqualene-lanosterol cyclase	Homo sapiens (human)	Baraitser-Winter syndrome Fabry disease Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Q fever Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome Wolman disease acquired immunodeficiency syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia alopecia-mental retardation syndrome 4 alopecia ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis blindness bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system cancer childhood acute lymphocytic leukemia childhood osteosarcoma chylomicron retention disease coronary artery disease diffuse idiopathic skeletal hyperostosis embryoma endometrial serous adenocarcinoma epilepsy epithelioid sarcoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma high grade glioma holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hypertension hypotrichosis 14 hypotrichosis 1 hypotrichosis intellectual disability learning disability lipid storage disease microcephaly mixed glioma orofaciodigital syndrome I orofaciodigital syndrome X ossification of the posterior longitudinal ligament of spine osteosarcoma ovary serous adenocarcinoma primary sclerosing cholangitis sarcoma sclerosing cholangitis senile cataract skin disease spinal stenosis spindle cell sarcoma squamous cell carcinoma tongue cancer tongue squamous cell carcinoma trypanosomiasis typhus visual epilepsy
9382	component of oligomeric golgi complex 1	COG1 Aliases: KIAA1381	Homo sapiens (human)	Baraitser-Winter syndrome Burkitt lymphoma Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome anemia branchiootic syndrome cerebral degeneration cerebrocostomandibular syndrome chronic lymphocytic leukemia clubfoot congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIg cryptorchidism hematologic cancer hydronephrosis hypospadias kidney failure macrocytic anemia orofaciodigital syndrome I orofaciodigital syndrome X placental insufficiency primary pulmonary hypertension scoliosis sensorineural hearing loss thrombocytopenia
1836	solute carrier family 26 member 2	SLC26A2 Aliases: DTDST diastrophic dysplasia sulfate transporter	Homo sapiens (human)	Baraitser-Winter syndrome Bartter disease Clostridium difficile colitis Conn's syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pendred Syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome achondrogenesis type IB achondroplasia adenocarcinoma adenoma arthritis arthropathy atelosteogenesis auditory system disease autosomal recessive osteopetrosis 7 benign mesothelioma brachydactyly branchiootic syndrome breast cancer cancer chondrodysplasia punctata cleft palate clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure cryptorchidism cystic lymphangioma diarrhea diastrophic dysplasia disease of metabolism dyshormonogenic goiter embryoma endometritis fibrosarcoma follicular adenoma inguinal hernia irritable bowel syndrome isolated cleft palate juvenile rheumatoid arthritis large intestine cancer laryngostenosis lingual-facial-buccal dyskinesia lung benign neoplasm lung cancer lung non-small cell carcinoma malignant mesothelioma mastitis microcystic adenoma movement disease mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia 4 multiple epiphyseal dysplasia neurocirculatory asthenia omphalocele orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis otosclerosis papillary adenoma placental insufficiency polyhydramnios primary hyperaldosteronism scoliosis sensorineural hearing loss spinal cord disease spondylolysis stomach cancer stomach carcinoma umbilical hernia
4595	mutY DNA glycosylase	MUTYH Aliases: MYH	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Hantavirus hemorrhagic fever with renal syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lynch syndrome Muir-Torre syndrome Peutz-Jeghers syndrome acoustic neuroma adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma age related macular degeneration anal carcinoma in situ angiomatous meningioma arthritis arthropathy benign meningioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral convexity meningioma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma chromosome 10q23 deletion syndrome clear cell meningioma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 2 familial adenomatous polyposis female breast carcinoma fibrous meningioma follicular adenoma gastroenteritis gastrointestinal system cancer gastrointestinal system disease gliosarcoma granular cell carcinoma hair follicle neoplasm head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile polyposis syndrome large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma myeloproliferative neoplasm nervous system cancer neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurotic disorder obsolete melancholia olfactory groove meningioma osteoarthritis ovarian cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma parasagittal meningioma pilomatrixoma pituitary adenoma primary open angle glaucoma proctitis prostate cancer prostate carcinoma psammomatous meningioma rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis sarcomatoid carcinoma sebaceous adenocarcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma in situ stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma transitional meningioma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer von Hippel-Lindau disease
176	aggrecan	ACAN Aliases: CSPGCP aggrecan proteoglycan	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Lyme disease Marfan syndrome SADDAN Silverman-Handmaker type dyssegmental dysplasia Werner syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia actinic keratosis amyloidosis anthracosilicosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bagassosis bicuspid aortic valve disease bone disease cancer cardiovascular system disease carpal tunnel syndrome cartilage disease cerebral infarction cerebrovascular disease cherubism chondroblastoma chondromalacia chondrosarcoma chordoma chorioamnionitis chronic interstitial cystitis ciliary body disease colon cancer colonic benign neoplasm colorectal cancer congestive heart failure connective tissue disease coronary artery disease degenerative disc disease dental fluorosis developmental and epileptic encephalopathy 39 diabetic ketoacidosis distal myopathy enterocele epithelioid sarcoma exostosis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy heart disease hepatocellular carcinoma hereditary multiple exostoses hypochondroplasia hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease infantile myofibromatosis interstitial cystitis iris disease juvenile rheumatoid arthritis large intestine cancer laryngeal carcinoma laryngeal disease larynx cancer limb-girdle muscular dystrophy lipoma liver cancer mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia multiple sclerosis multiple symmetric lipomatosis muscular dystrophy neurogenic arthropathy nicotine dependence obesity obsessive-compulsive disorder obsessive-compulsive personality disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoarthritis osteochondritis dissecans osteochondrodysplasia osteogenesis imperfecta panuveitis periarthritis peroxisome biogenesis disorder 5A pleomorphic lipoma pneumoconiosis polycystic ovary syndrome progeria progressive pseudorheumatoid arthropathy of childhood prune belly syndrome pseudoachondroplasia reticulate acropigmentation of Kitamura rheumatoid arthritis sarcoma schizophrenia scoliosis septic arthritis siderosis situs inversus spindle cell sarcoma spondylitis spondyloarthropathy spondyloepiphyseal dysplasia Kimberley type spondyloepiphyseal dysplasia congenita spondylosis status epilepticus tendinitis tracheal disease tropical spastic paraparesis tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus uveitis
1298	collagen type IX alpha 2 chain	COL9A2 Aliases: MED	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
6392	succinate dehydrogenase complex subunit D	SDHD Aliases: cybS small subunit of cytochrome b	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Carney-Stratakis syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Cowden syndrome Laron syndrome Peutz-Jeghers syndrome Stevens-Johnson syndrome Unverricht-Lundborg syndrome X-linked dilated cardiomyopathy achondroplasia acoustic neuroma actinic keratosis acute promyelocytic leukemia adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma agnosia allergic asthma amnestic disorder angiomatous meningioma aniridia anxiety disorder asthma attention deficit hyperactivity disorder autistic disorder benign meningioma blepharospasm blindness breast cancer breast carcinoma cancer capillary hemangioma cardiomyopathy cataract 4 multiple types cavernous hemangioma central nervous system cancer cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chorioangioma chromophobe renal cell carcinoma clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common cold cone-rod dystrophy congenital nystagmus congenital ptosis congestive heart failure cranial nerve disease cranial nerve palsy cutaneous fibrous histiocytoma deafness-dystonia-optic neuronopathy syndrome dementia depressive disorder developmental coordination disorder differentiated thyroid gland carcinoma dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy dissociated nystagmus duodenum cancer dysthymic disorder dystonia early myoclonic encephalopathy embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy exanthem familial hypertrophic cardiomyopathy fibrous meningioma fissured tongue focal hand dystonia fundus albipunctatus gastrointestinal stromal tumor gastrointestinal system cancer generalized anxiety disorder geographic tongue gliosarcoma glomangioma glomerulonephritis glomus tumor goiter growth hormone secreting pituitary adenoma gynecomastia heart cancer hemangioma hepatocellular carcinoma hidradenoma high grade glioma histiocytoid hemangioma hypercalcemia hypertensive retinopathy hypertrophic cardiomyopathy hypertrophy of breast ileus infant gynecomastia insulinoma intellectual disability intestinal obstruction intramuscular hemangioma intraorbital meningioma intraventricular meningioma intrinsic asthma inverted follicular keratosis keratoacanthoma keratosis kidney cancer kidney disease large intestine cancer learning disability left ventricular noncompaction leprosy lipoma liver cancer lymphangioma major depressive disorder melancholic depression melanoacanthoma melanoma meningioma meningothelial meningioma microcephaly microcystic meningioma mitochondrial complex II deficiency mixed glioma mononeuritis multiplex mononeuritis mononeuropathy multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A myopia nephritis nephrocalcinosis neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis 1 neurofibromatosis neurotic disorder nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma nontoxic goiter obsolete intestinal pseudo-obstruction obsolete melancholia ocular melanoma olfactory groove meningioma ophthalmoplegia optic atrophy palmoplantar keratosis papillary renal cell carcinoma papilloma paraganglioma paralytic ileus parasagittal meningioma pathologic nystagmus pheochromocytoma phobic disorder phosphorus metabolism disease pituitary adenoma placental insufficiency pleomorphic lipoma primary autosomal recessive microcephaly 1 proteinuria psammomatous meningioma ptosis pulmonary large cell neuroendocrine carcinoma renal artery obstruction renal carcinoma renal cell carcinoma renal osteodystrophy retinitis pigmentosa retinoblastoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis seborrheic keratosis secretory meningioma sensorineural hearing loss skin disease skin melanoma skin papilloma skin tag small intestine cancer spinal meningioma spontaneous ocular nystagmus squamous cell papilloma stomach cancer stomach carcinoma syringoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma thyroid gland medullary carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tuberculosis tuberous sclerosis uterine corpus cancer uveal melanoma visual epilepsy von Hippel-Lindau disease
6391	succinate dehydrogenase complex subunit C	SDHC Aliases: CYB560 cybL large subunit of cytochrome b succinate dehydrgenase cytochrome b succinate dehydrogenase cytochrome b560 subunit	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Carney complex Carney-Stratakis syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Cowden syndrome Laron syndrome Leigh disease Peutz-Jeghers syndrome Raynaud disease achondroplasia achromatopsia acoustic neuroma acquired color blindness adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland cancer anemia angioedema angiomatous meningioma aniridia autistic disorder autosomal dominant cerebellar ataxia benign meningioma bipolar disorder blue color blindness bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer capillary hemangioma cataract 4 multiple types cataract cavernous hemangioma central nervous system cancer cerebral convexity meningioma childhood osteosarcoma choriocarcinoma chromophobe renal cell carcinoma clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma congestive heart failure cranial nerve disease cranial nerve palsy cutaneous fibrous histiocytoma duodenum cancer embryoma endocrine gland cancer endometrial cancer endometrial carcinoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exanthem fibrous meningioma fissured tongue follicular adenoma gangliocytoma ganglioneuroma gastrointestinal stromal tumor gastrointestinal system cancer geographic tongue gestational diabetes gliosarcoma glomerulonephritis goiter gynecomastia head and neck cancer heart cancer hemangioma hepatitis C hepatocellular carcinoma hidradenoma high grade glioma hypercalcemia hypertension hypertensive retinopathy hypertrophy of breast ileus infant gynecomastia intellectual disability intestinal obstruction intracranial hypertension intraorbital meningioma intraventricular meningioma kidney disease large intestine cancer learning disability lipoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma macrocytic anemia melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mitochondrial metabolism disease mitochondrial myopathy mixed glioma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A myopia nephritis nephrocalcinosis neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibroma neurofibromatosis 1 neurofibromatosis nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma nontoxic goiter obsolete constipation olfactory groove meningioma osteosarcoma palmoplantar keratosis panic disorder papillary adenoma papillary renal cell carcinoma papilloma paraganglioma parasagittal meningioma peripheral nervous system neoplasm pheochromocytoma phosphorus metabolism disease pituitary adenoma placenta cancer pleomorphic lipoma primary hyperparathyroidism prostate cancer prostate carcinoma proteinuria psammomatous meningioma pseudotumor cerebri rectal benign neoplasm rectum cancer red color blindness red-green color blindness renal carcinoma renal cell carcinoma renal osteodystrophy sarcoma sarcomatoid renal cell carcinoma scleroderma scoliosis secretory meningioma sensorineural hearing loss skin melanoma skin papilloma skin tag small intestine benign neoplasm small intestine cancer spinal meningioma spindle cell sarcoma spinocerebellar ataxia type 2 squamous cell papilloma stomach cancer stomach carcinoma syringoma systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma thyroid gland medullary carcinoma transitional meningioma tuberous sclerosis urticaria uterine corpus cancer visual epilepsy von Hippel-Lindau disease
8807	interleukin 18 receptor accessory protein	IL18RAP Aliases: AcPL CD218b	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Burkitt lymphoma Cowden syndrome Crohn's colitis Crohn's disease Graves' disease Richter's syndrome allergic asthma asthma autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis bone marrow disease cancer cardiovascular system disease celiac disease cerebral infarction cerebrovascular disease chronic lymphocytic leukemia degenerative disc disease diabetic ketoacidosis esophageal disease essential hypertension goiter heart disease hypertension hyperthyroidism immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma obsolete type 1 diabetes mellitus 9 rheumatoid arthritis spinal cord disease stomach disease syringomyelia systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus ulcerative colitis
9469	carbohydrate sulfotransferase 3	CHST3 Aliases: C6ST C6ST1 chondroitin 6 sulfotransferase 1	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
54965	phosphatidylinositol glycan anchor biosynthesis class X	PIGX Aliases: FLJ20522 PIG-X	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Laurence-Moon syndrome allergic asthma allergic disease asthma breast cancer breast carcinoma cancer dermatitis embryoma intrinsic asthma polydactyly
56623	inositol polyphosphate-5-phosphatase E	INPP5E Aliases: CORS1 PPI5PIV Phosphatidylinositol polyphosphate 5-phosphatase type IV pharbin	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
9993	DiGeorge syndrome critical region gene 2	DGCR2 Aliases: DGS-C IDD KIAA0163 LAN SEZ-12 integral membrane protein DGCR2	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Baraitser-Winter syndrome Cowden syndrome DiGeorge syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Nezelof syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia acromegaly acute myocardial infarction adrenal gland cancer amyloidosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bipolar disorder blepharophimosis branchiootic syndrome cancer cervix disease chronic interstitial cystitis congenital heart disease coronary thrombosis craniosynostosis degenerative disc disease delusional disorder diabetes mellitus diabetic ketoacidosis double outlet right ventricle duodenum cancer embryoma epilepsy heart cancer hyperpituitarism hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism immune system disease intellectual disability interstitial cystitis learning disability microcephaly myocardial infarction myotonic dystrophy type 1 neuroblastoma obsolete type 1 diabetes mellitus 9 orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia pheochromocytoma primary biliary cholangitis prune belly syndrome pseudohypoparathyroidism schizophrenia silent myocardial infarction small intestine cancer type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus velocardiofacial syndrome ventricular septal defect visual epilepsy
266722	heparan sulfate 6-O-sulfotransferase 3	HS6ST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer central nervous system disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy hepatitis B narcolepsy nicotine dependence obesity type 2 diabetes mellitus
4245	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT1 Aliases: GLCNAC-TI GNT-1 GnTI	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease central nervous system cancer central nervous system disease complex partial epilepsy congestive heart failure cystinuria diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism embryoma endomyocardial fibrosis epilepsy galactokinase deficiency galactosemia gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycine encephalopathy glycogen storage disease Ia glycogen storage disease heart disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease liver cancer mixed glioma multiple sclerosis narcolepsy nervous system disease obesity obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder temporal lobe epilepsy type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus visual epilepsy
9348	N-deacetylase and N-sulfotransferase 3	NDST3 Aliases: HSST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder autism spectrum disorder azoospermia central nervous system disease depressive disorder generalized anxiety disorder intellectual disability major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
161357	MAM domain containing glycosylphosphatidylinositol anchor 2	MDGA2	Homo sapiens (human)	Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy benign epilepsy with centrotemporal spikes cancer central nervous system disease dissociative disorder embryoma microinvasive gastric cancer narcolepsy neurotic disorder rheumatoid arthritis sexual dysfunction stomach cancer stomach carcinoma systemic lupus erythematosus
60506	nyctalopin	NYX Aliases: CLRP CSNB1A	Homo sapiens (human)	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
2262	glypican 5	GPC5 Aliases: glypican proteoglycan 5	Homo sapiens (human)	Balo concentric sclerosis Gilles de la Tourette syndrome MHC class II deficiency Marfan syndrome Simpson-Golabi-Behmel syndrome type 1 adenosine deaminase deficiency adrenoleukodystrophy bronchus cancer bronchus carcinoma cancer cardiac arrest cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types central nervous system cancer central nervous system disease central nervous system lymphoma demyelinating disease diabetes mellitus epithelioid sarcoma familial nephrotic syndrome gliosarcoma glomerulonephritis hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma microphthalmia mixed glioma multiple sclerosis myelomeningocele narcolepsy nephritis nephrotic syndrome neuromyelitis optica obsolete Matthew-Wood syndrome obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma proteinuria rhabdomyosarcoma rheumatoid arthritis sarcoma scoliosis severe combined immunodeficiency situs inversus spina bifida spindle cell sarcoma tethered spinal cord syndrome tetralogy of Fallot transthyretin amyloidosis tuberous sclerosis type 2 diabetes mellitus
411	arylsulfatase B	ARSB Aliases: ASB	Homo sapiens (human)	Balo concentric sclerosis Fabry disease Laron syndrome Machado-Joseph disease Scheie syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cardiomyopathy carotid artery disease central nervous system disease chondrodysplasia punctata chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis embryoma endomyocardial fibrosis essential hypertension glaucoma glycogen storage disease II hydrocephalus hypertension hypertrichosis hypertrophic cardiomyopathy inguinal hernia large intestine cancer lipid storage disease lung benign neoplasm lysosomal storage disease melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myocarditis narcolepsy nervous system disease obstructive hydrocephalus omphalocele osteochondrodysplasia osteonecrosis prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder senile degeneration of brain sensorineural hearing loss skin melanoma spinal cord disease tuberculosis umbilical hernia
1375	carnitine palmitoyltransferase 1B	CPT1B Aliases: CPT1-M M-CPT1 carnitine O-palmitoyltransferase 1B	Homo sapiens (human)	Balo concentric sclerosis Down syndrome Pearson syndrome acute myocardial infarction adrenoleukodystrophy bladder carcinoma cancer central nervous system disease chronic recurrent multifocal osteomyelitis colitis congestive heart failure coronary thrombosis embryoma gastroenteritis hepatitis hepatocellular carcinoma ileitis ileocolitis liver cancer morbid obesity myocardial infarction narcolepsy post-traumatic stress disorder restless legs syndrome silent myocardial infarction steatotic liver disease systemic primary carnitine deficiency disease urinary bladder cancer very long chain acyl-CoA dehydrogenase deficiency

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