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 **1426 - 1450** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
1645	aldo-keto reductase family 1 member C1	AKR1C1 Aliases: DD1 DDH HAKRC MBAB dihydrodiol dehydrogenase 1; 20-alpha (3-alpha)-hydroxysteroid dehydrogenase	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis Marfan syndrome T-cell acute lymphoblastic leukemia X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta anxiety disorder arthritis arthropathy benign mesothelioma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cervical cancer childhood germ cell cancer childhood osteosarcoma clear cell adenocarcinoma clubfoot colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma common wart dentin dysplasia dentinogenesis imperfecta disorder of sexual development embryoma embryonal cancer endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of ovary endometriosis of uterus endometriosis esophagus squamous cell carcinoma gallbladder disease generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma head and neck squamous cell carcinoma hepatocellular carcinoma hermaphroditism large intestine cancer liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoma malignant mesothelioma non-Hodgkin lymphoma obesity obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma panic disorder parapsoriasis phobic disorder polycystic ovary syndrome prostate cancer prostate carcinoma pseudohermaphroditism psoriasis pustulosis of palm and sole reticulosarcoma situs inversus squamous cell carcinoma tongue squamous cell carcinoma tuberous sclerosis urinary bladder cancer uterine corpus cancer
145173	beta 3-glucosyltransferase	B3GLCT Aliases: B3GTL B3Glc-T beta-1,3-glucosyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome IGSF1 deficiency syndrome Klippel-Feil syndrome Kuhnt-Junius degeneration Meckel syndrome Peters anomaly Peters plus syndrome Tn polyagglutination syndrome age related macular degeneration anemia 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 autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease blindness cataract cerebral degeneration cleft lip cleft palate coloboma communicating hydrocephalus congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus congenital ptosis cornea plana craniosynostosis cryptorchidism degeneration of macula and posterior pole depressive disorder dissociated nystagmus epilepsy eye disease glaucoma heart septal defect hydrocephalus hydronephrosis hypoplastic left heart syndrome hypospadias hypothyroidism imperforate anus inguinal hernia intellectual disability isolated cleft palate learning disability macrocytic anemia macular degeneration major depressive disorder melancholic depression microcephaly myopia myxedema obsolete melancholia obstructive hydrocephalus omphalocele optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus placental insufficiency polyhydramnios popliteal pterygium syndrome ptosis pulmonary valve stenosis recurrent corneal erosion renal hypoplasia scoliosis senile degeneration of brain sensorineural hearing loss spina bifida occulta spondylolisthesis spontaneous ocular nystagmus syndactyly trichohepatoenteric syndrome 1 trichohepatoenteric syndrome umbilical hernia ventricular septal defect visual epilepsy
8850	lysine acetyltransferase 2B	KAT2B	Homo sapiens (human)	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
11091	WD repeat domain 5	WDR5	Homo sapiens (human)	congenital heart disease
3423	iduronate 2-sulfatase	IDS Aliases: Hunter syndrome ID2S	Homo sapiens (human)	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
5373	phosphomannomutase 2	PMM2 Aliases: CDG1a CDGS Congenital disorder of glycosylation, type Ia PMI PMI1 mannose-6-phosphate isomerase phosphomannose isomerase 1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Dandy-Walker syndrome Duchenne muscular dystrophy Hailey-Hailey disease Kallmann syndrome Marfan syndrome Meckel syndrome Pick's disease Reye syndrome Rothmund-Thomson syndrome Sheehan syndrome West syndrome Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction androgen insensitivity syndrome antithrombin III deficiency anxiety disorder aspiration pneumonia aspiration pneumonitis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 dominant polycystic kidney disease autosomal recessive chronic granulomatous disease 1 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 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 blindness brain ischemia cancer cardiomyopathy cardiovascular system disease cataract cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy chronic granulomatous disease clubfoot coloboma of optic nerve colorectal cancer colorectal carcinoma cone-rod dystrophy congenital diaphragmatic hernia congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Id congenital disorder of glycosylation Ie congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypothyroidism congenital muscular dystrophy congenital nystagmus coronary thrombosis critical illness polyneuropathy cryptorchidism cutis laxa cystic kidney disease developmental and epileptic encephalopathy 36 diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diarrhea disease of metabolism dissociated nystagmus distal myopathy egg allergy elephantiasis embryoma endomyocardial fibrosis epilepsy esotropia essential hypertension facioscapulohumeral muscular dystrophy familial hemiplegic migraine 1 familial hemiplegic migraine familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hypertrophic cardiomyopathy familial nephrotic syndrome fundus albipunctatus gallbladder disease generalized anxiety disorder heart disease hemiplegia hemopericardium hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypertropia hypogonadism 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 inflammatory and toxic neuropathy inherited metabolic disorder intellectual disability 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 large intestine cancer learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lipoid nephrosis liver cirrhosis liver disease lung adenocarcinoma lung cancer lymphedema mal de Meleda marasmus mechanical strabismus meningoencephalitis microcephaly migraine with aura monocular esotropia movement disease muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopia myxedema nephrotic syndrome neuropathy non-congenital cyst of kidney 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 infantile epileptic encephalopathy oculopharyngeal muscular dystrophy olivopontocerebellar atrophy open-angle glaucoma ophthalmoplegia osteoporosis panhypopituitarism pathologic nystagmus pericardial effusion pericarditis peripheral nervous system disease periventricular leukomalacia phobic disorder polyhydramnios polyneuropathy premature menopause primary open angle glaucoma primary ovarian insufficiency protein C deficiency protein S deficiency proteinuria pulmonary valve stenosis restrictive dermopathy retinitis pigmentosa rippling muscle disease 2 schizophrenia scoliosis silent myocardial infarction situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus steatotic liver disease strabismus thrombocytopenia thrombocytosis thrombophilia tuberous sclerosis type 2 diabetes mellitus visual epilepsy visual pathway disease
2531	3-ketodihydrosphingosine reductase	KDSR Aliases: 3-dehydrosphinganine reductase DHSR SDR35C1 short chain dehydrogenase/reductase family 35C, member 1	Homo sapiens (human)	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Laron syndrome achondroplasia actinic keratosis alopecia blood platelet disease cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis et progressiva 4 erythrokeratodermia variabilis exanthem follicular lymphoma glaucoma granuloma annulare intellectual disability learning disability liver disease microcephaly nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma obsolete ymphosarcoma palmoplantar keratosis papillary renal cell carcinoma photosensitive epilepsy photosensitivity disease progressive muscular atrophy recurrent corneal erosion renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis sensorineural hearing loss skin benign neoplasm skin cancer skin disease spinal muscular atrophy steatotic liver disease thrombocytopenia
55650	phosphatidylinositol glycan anchor biosynthesis class V	PIGV Aliases: FLJ20477 GPI mannosyltransferase 2 GPI-MT-II PIG-V dol-P-Man dependent GPI mannosyltransferase II	Homo sapiens (human)	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome anorectal stricture blepharospasm capillary disease congenital heart disease craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 1 intellectual disability learning disability monocular esotropia oligohydramnios pyridoxine deficiency anemia scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
113829	solute carrier family 35 member A4	SLC35A4	Homo sapiens (human)	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
5162	pyruvate dehydrogenase E1 subunit beta	PDHB Aliases: E1beta PDHE1B	Homo sapiens (human)	Leigh disease acute myocardial infarction breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis diabetes mellitus lactic acidosis luminal breast carcinoma A melanoma myocardial infarction nonpapillary renal cell carcinoma papillary adenocarcinoma papillary renal cell carcinoma pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma thyroid gland papillary carcinoma type 2 diabetes mellitus
32	acetyl-CoA carboxylase beta	ACACB Aliases: ACACbeta ACC-beta ACC2 ACCB ACCbeta HACC275 acetyl-CoA carboxylase 2	Homo sapiens (human)	B-cell lymphoma Clostridium difficile colitis Clouston syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction adenoid cystic carcinoma arteriosclerotic cardiovascular disease atherosclerosis cancer carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis head and neck squamous cell carcinoma high grade glioma hypopharynx cancer kidney disease large intestine cancer major depressive disorder metabolic dysfunction-associated steatotic liver disease morbid obesity muscular disease myocardial infarction nephritis nephrosis neurotic disorder nutmeg liver obesity obsolete ymphosarcoma pancreatic ductal adenocarcinoma perinatal necrotizing enterocolitis pyoureter salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma silent myocardial infarction steatotic liver disease type 2 diabetes mellitus viral infectious disease
142827	acyl-CoA synthetase medium chain family member 6	ACSM6 Aliases: bA310E22.3	Homo sapiens (human)
1118	chitinase 1	CHIT1 Aliases: CHI3 CHIT chitotriosidase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bloch-Sulzberger syndrome Creutzfeldt-Jakob disease Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Wolman disease acute myeloid leukemia adrenoleukodystrophy alkaptonuria allergic asthma allergic rhinitis amyloidosis amyotrophic lateral sclerosis ancylostomiasis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis aspartylglucosaminuria asthma atherosclerosis bacterial sepsis beta thalassemia bone marrow cancer breast cancer breast carcinoma cancer carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease childhood type dermatomyositis cholestasis chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency coronary artery disease cryptococcosis cystic fibrosis dementia dermatomyositis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia eumycotic mycetoma familial combined hyperlipidemia familial mediterranean fever filariasis follicular lymphoma frontotemporal dementia fucosidosis gastritis glomerulonephritis glycoproteinosis hepatitis C hypomelanosis of Ito idiopathic interstitial pneumonia interstitial lung disease intrinsic asthma juvenile rheumatoid arthritis kidney disease large intestine cancer lipid storage disease liver cirrhosis lung disease lysosomal acid lipase deficiency lysosomal storage disease malaria mevalonic aciduria multiple sclerosis myelofibrosis myeloproliferative neoplasm nephritis nephrosis neurodegenerative disease neuropathy nodal marginal zone lymphoma nutmeg liver obesity obstructive sleep apnea ochronosis osteoarthritis peripheral nervous system disease plasmacytoma polycythemia vera polycythemia polyneuropathy postinflammatory pulmonary fibrosis progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pulmonary fibrosis pyoureter sarcoidosis sialuria sickle cell anemia sphingolipidosis steatotic liver disease thalassemia tuberculosis type 2 diabetes mellitus uveoparotid fever vascular dementia vasomotor rhinitis
27255	contactin 6	CNTN6 Aliases: NB-3 neural adhesion molecule	Homo sapiens (human)	Gilles de la Tourette syndrome Hirschsprung's disease Parkinson's disease 2 acquired immunodeficiency syndrome adenoid cystic carcinoma alcohol dependence alcohol use disorder anorexia nervosa attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder breast cancer communicating hydrocephalus cone-rod dystrophy 2 cone-rod dystrophy differentiated thyroid gland carcinoma epilepsy hydrocephalus intellectual disability learning disability obstructive hydrocephalus ovarian carcinoma salivary gland adenoid cystic carcinoma schizophrenia senile degeneration of brain systemic lupus erythematosus
8509	N-deacetylase and N-sulfotransferase 2	NDST2 Aliases: HSST2 NST2	Homo sapiens (human)	autism spectrum disorder azoospermia intellectual disability prostate cancer prostate carcinoma
284369	SIGLEC family like 1	SIGLECL1 Aliases: FLJ40235	Homo sapiens (human)
10026	phosphatidylinositol glycan anchor biosynthesis class K	PIGK Aliases: GPI transamidase subunit GPI-anchor transamidase GPI8 GPI8 homolog (S. cerevisiae) PIG-K hGPI8	Homo sapiens (human)	adult lymphoma cancer central nervous system lymphoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lymphoma obsolete ymphosarcoma
11332	acyl-CoA thioesterase 7	ACOT7 Aliases: ACH1 ACT BACH CTE-II LACH1 Long chain acyl-CoA thioester hydrolase MGC1126 brain acyl CoA hydrolase hBACH	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clouston syndrome Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium vivax malaria Reye syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation bacterial infectious disease beta thalassemia blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health distal arthrogryposis dysentery dysthymic disorder eating disorder embryoma epilepsy esophagus squamous cell carcinoma female stress incontinence gallbladder disease gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inclusion body myositis infertility intrinsic asthma kwashiorkor large intestine cancer leprosy liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malaria marasmus melancholic depression mixed glioma multiple sclerosis muscular dystrophy myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nonpapillary renal cell carcinoma nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease osteomyelitis ovarian cancer ovarian carcinoma papillary renal cell carcinoma peripheral nervous system disease peroxisome biogenesis disorder 7A pertussis polyneuropathy postpartum depression pre-eclampsia prediabetes syndrome primary open angle glaucoma primary ovarian insufficiency primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition psychotic disorder pulmonary tuberculosis renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma sick sinus syndrome silent myocardial infarction spermatic cord torsion systemic scleroderma temporal lobe epilepsy thalassemia tuberculosis tuberculous pneumothorax tubular adenocarcinoma 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 urethral intrinsic sphincter deficiency viral infectious disease visual epilepsy
5833	phosphate cytidylyltransferase 2, ethanolamine	PCYT2 Aliases: CTP:phosphoethanolamine cytidylyltransferase ET ethanolamine-phosphate cytidylyltransferase: phosphorylethanolamine transferase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cerebral degeneration embryoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 82 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia
6484	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	ST3GAL4 Aliases: FLJ11867 SAT3 ST3Gal IV STZ	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder 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 brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma 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 melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma 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
1943	ephrin A2	EFNA2 Aliases: ELF-1 EPH-related receptor tyrosine kinase ligand 6 LERK6	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma chronic granulomatous disease embryoma endometrial cancer endometrial carcinoma familial retinoblastoma gastrointestinal system cancer giant cell glioblastoma glioblastoma high grade glioma lupus erythematosus nasopharynx carcinoma nodular prostate pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma prostatic adenoma retinoblastoma stomach cancer stomach carcinoma systemic lupus erythematosus trilateral retinoblastoma uterine corpus cancer
7369	uromodulin	UMOD Aliases: Tamm-Horsfall glycoprotein uromucoid	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fabry disease IgA glomerulonephritis Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Senior-Loken syndrome Van der Woude syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute pancreatitis adenine phosphoribosyltransferase deficiency adult acute lymphocytic leukemia alcohol dependence alcohol use disorder anxiety disorder aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune hepatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease babesiosis bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic interstitial cystitis chronic kidney disease chronic pyelonephritis chylomicron retention disease cleidocranial dysplasia cocaine abuse cocaine dependence congestive heart failure coronary artery disease cystic kidney disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma esophageal cancer esophageal carcinoma essential hypertension familial juvenile hyperuricemic nephropathy gallbladder disease generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance gout heart disease hepatitis A hepatitis humeroradial synostosis hypertension hyperuricemia interstitial cystitis interstitial nephritis kidney disease kidney failure leukemia lipid storage disease liver cirrhosis liver disease lupus erythematosus maple syrup urine disease middle cerebral artery infarction morphine dependence nephritis nephrolithiasis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis normal pressure hydrocephalus nutmeg liver obsolete type 1 diabetes mellitus 9 osteoporosis ovarian cancer ovarian carcinoma pancreatitis pertussis phobic disorder polycystic kidney disease 1 polycystic kidney disease 4 polydactyly prediabetes syndrome pyelitis pyelonephritis pyoureter radioulnar synostosis renal hypertension renal infectious disease secondary hyperparathyroidism systemic lupus erythematosus tuberculosis 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 uremia uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction
10237	solute carrier family 35 member B1	SLC35B1 Aliases: ATP/ADP exchanger in the ER membrane AXER UGTREL1	Homo sapiens (human)
160851	diacylglycerol kinase eta	DGKH Aliases: DGKeta	Homo sapiens (human)	allergic asthma asthma attention deficit hyperactivity disorder bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma disease of mental health esophageal cancer esophageal carcinoma intermittent explosive disorder intrinsic asthma lung benign neoplasm lung cancer lung carcinoma melancholic depression mood disorder nephrolithiasis neurotic disorder obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia panic disorder psychotic disorder schizophrenia uric acid nephrolithiasis
139189	diacylglycerol kinase kappa	DGKK	Homo sapiens (human)	Marfan syndrome agnosia arteriosclerotic cardiovascular disease atherosclerosis conduct disorder coronary artery disease developmental coordination disorder disease of mental health fragile X syndrome hepatocellular carcinoma hypospadias liver cancer prostate cancer prostate carcinoma situs inversus syndromic X-linked intellectual disability 94 tuberous sclerosis

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