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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 .

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 **76 - 100** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
417	ADP-ribosyltransferase 1	ART1 Aliases: ART2 ARTC1 CD296	Homo sapiens (human)	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
419	ADP-ribosyltransferase 3 (inactive)	ART3 Aliases: ARTC3	Homo sapiens (human)	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
420	ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)	ART4 Aliases: ARTC4 CD297 DOK1 NAD(+)--protein-arginine ADP-ribosyltransferase 4	Homo sapiens (human)	carotid artery thrombosis carotid stenosis conjunctivitis
427	N-acylsphingosine amidohydrolase 1	ASAH1 Aliases: AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase	Homo sapiens (human)	Albright's hereditary osteodystrophy 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 Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency 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 cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder sphingolipidosis spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
432	asialoglycoprotein receptor 1	ASGR1 Aliases: CLEC4H1	Homo sapiens (human)	acrodermatitis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease dermatitis hepatocellular carcinoma liver cancer nutmeg liver thrombocytopenia
433	asialoglycoprotein receptor 2	ASGR2 Aliases: CLEC4H2	Homo sapiens (human)
467	activating transcription factor 3	ATF3	Homo sapiens (human)	prostate cancer pulmonary tuberculosis
468	activating transcription factor 4	ATF4	Homo sapiens (human)	borna disease prostate carcinoma pulmonary venoocclusive disease
477	ATPase Na+/K+ transporting subunit alpha 2	ATP1A2	Homo sapiens (human)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
501	aldehyde dehydrogenase 7 family member A1	ALDH7A1 Aliases: 26g turgor protein homolog EPD P6c dehydrogenase PDE alpha-AASA dehydrogenase alpha-aminoadipic semialdehyde dehydrogenase antiquitin 1 delta1-piperideine-6-carboxylate dehydrogenease	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 Balo concentric sclerosis Becker muscular dystrophy Dravet syndrome Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pendred Syndrome Pick's disease Reye syndrome Richter's syndrome Usher syndrome type 1 Usher syndrome acrodermatitis adrenoleukodystrophy adult respiratory distress syndrome allergic asthma asphyxia neonatorum asthma atopic dermatitis 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 bone disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cartilage disease 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 disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholera chronic lymphocytic leukemia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congestive heart failure connective tissue disease depressive disorder dermatitis developmental and epileptic encephalopathy 2 diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health distal myopathy dyshormonogenic goiter dysthymic disorder early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset vitamin B6-dependent epilepsy 4 embryoma endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy fundus albipunctatus gastrointestinal stromal tumor giant cell glioblastoma glaucoma glioblastoma heart disease hepatitis C hepatocellular carcinoma high grade glioma homocystinuria hydrocephalus hyperprolinemia type 2 hypertension hypertropia hypophosphatasia impotence intellectual disability intermittent claudication intrinsic asthma keratosis follicularis lactic acidosis large intestine cancer learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma major depressive disorder mechanical strabismus melancholic depression melanoma microphthalmia mongolian spot movement disease muscular dystrophy narcolepsy nervous system disease neurotic disorder newborn respiratory distress syndrome nodular prostate obsolete Dravet syndrome obsolete Matthew-Wood syndrome 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 obsolete melancholia oculopharyngeal muscular dystrophy open-angle glaucoma ophthalmoplegia osteoporosis peripheral artery disease peripheral vascular disease pigment dispersion syndrome pneumonia premature ejaculation primary pulmonary hypertension prostate cancer prostate carcinoma prostatic adenoma pseudoxanthoma elasticum psychologic dyspareunia psychotic disorder pyridoxine-dependent epilepsy rectal benign neoplasm rectum adenocarcinoma rectum cancer retinitis pigmentosa sarcomatoid carcinoma schizophrenia seminoma sexual dysfunction skin melanoma speech disorder squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma strabismus testicular cancer testicular germ cell cancer tongue squamous cell carcinoma type 2 diabetes mellitus visual epilepsy
523	ATPase H+ transporting V1 subunit A	ATP6V1A Aliases: V-ATPase subunit A V-type proton ATPase (V-ATPase) catalytic subunit A VA68 Vma1	Homo sapiens (human)	American histoplasmosis Dandy-Walker syndrome Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome achondroplasia agnosia angioma serpiginosum anodontia aspergillosis 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 attention deficit hyperactivity disorder autistic disorder autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID black piedra blepharophimosis blepharospasm brain disease capillary hemangioma cardiomyopathy cataract cavernous hemangioma cerebral degeneration clubfoot coccidioidomycosis coloboma colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital ptosis congestive heart failure cortical dysplasia-focal epilepsy syndrome cryptorchidism cutis laxa dementia dental caries dentin caries developmental and epileptic encephalopathy 93 developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy endomyocardial fibrosis entropion epilepsy esophagitis familial hypertrophic cardiomyopathy focal hand dystonia gastroesophageal reflux disease histoplasmosis hydranencephaly hyperopia hypertrophic cardiomyopathy hypertropia inguinal hernia intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy patent foramen ovale pathologic nystagmus peptic esophagitis placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 ptosis retinal degeneration schizophrenia septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly spontaneous ocular nystagmus sporotrichosis status epilepticus stomach cancer stomach carcinoma strabismus superficial mycosis syndromic X-linked intellectual disability Najm type tooth agenesis visual epilepsy white piedra
537	ATPase H+ transporting accessory protein 1	ATP6AP1 Aliases: 16A Ac45 CF2 ORF VATPS1 X-associated protein 3 XAP-3 XAP3 vacuolar ATPase subunit S1	Homo sapiens (human)	Hailey-Hailey disease Rothmund-Thomson syndrome 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 cancer congenital disorder of glycosylation cutis laxa exocrine pancreatic insufficiency follicular lymphoma gallbladder disease hyperopia immunodeficiency 47 leukopenia liver disease mal de Meleda restrictive dermopathy steatotic liver disease tuberculosis
570	bile acid-CoA:amino acid N-acyltransferase	BAAT Aliases: BAT glycine N-choloyltransferase	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome Graves' disease Hantavirus hemorrhagic fever with renal syndrome Lynch syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma atypical hemolytic-uremic syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial sepsis basal cell carcinoma blood coagulation disease breast cancer breast carcinoma cancer carcinoma cervical cancer cholestasis chondrodysplasia-pseudohermaphroditism syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism coronary thrombosis diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia fibroepithelial basal cell carcinoma follicular adenoma giant cell glioblastoma glioblastoma hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperthyroidism hypothyroidism infertility islet cell tumor large intestine cancer lipoma lung cancer lung non-small cell carcinoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma morbid obesity myelodysplastic syndrome myocardial infarction myxedema obesity obsolete inherited blood coagulation disease obsolete steatorrhea obsolete type 1 diabetes mellitus 9 osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteomalacia papillary adenoma pleomorphic lipoma pneumonia polycystic ovary syndrome prostate cancer prostate carcinoma rickets sarcomatoid carcinoma silent myocardial infarction steatotic liver disease stomach cancer stomach carcinoma thrombocytopenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyrotoxicosis 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 uterine corpus cancer von Willebrand's disease 1 von Willebrand's disease 3 von Willebrand's disease
572	BCL2 associated agonist of cell death	BAD	Homo sapiens (human)	Alzheimer's disease Parkinsonism acute kidney failure brain ischemia breast cancer colon cancer diabetic neuropathy endometrial cancer gastric ulcer glaucoma high grade glioma hypertension hypothyroidism impotence intermittent claudication lung non-small cell carcinoma macular degeneration middle cerebral artery infarction obesity osteoarthritis pancreatic cancer prostate carcinoma prostatic hypertrophy pulmonary fibrosis renal cell carcinoma traumatic brain injury type 2 diabetes mellitus visual epilepsy
593	branched chain keto acid dehydrogenase E1 subunit alpha	BCKDHA Aliases: MSU maple syrup urine disease	Homo sapiens (human)	Crohn's colitis Crohn's disease acute pancreatitis arthritis arthropathy bacterial sepsis brain edema cerebral infarction cerebrovascular disease epilepsy gout hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability lactic acidosis learning disability maple syrup urine disease pancreatitis placental insufficiency shigellosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome ulcerative colitis visual epilepsy
594	branched chain keto acid dehydrogenase E1 subunit beta	BCKDHB Aliases: 2-oxoisovalerate dehydrogenase subunit beta, mitochondrial maple syrup urine disease	Homo sapiens (human)	Alzheimer's disease 12 Kaposi's sarcoma acute pancreatitis androgen insensitivity syndrome brain edema cancer celiac disease embryoma epilepsy hepatitis B hepatocellular carcinoma hypoglycemia intellectual disability lactic acidosis learning disability liver cancer maple syrup urine disease pancreatic cancer pancreatic carcinoma pancreatitis premature menopause primary ovarian insufficiency systemic lupus erythematosus thyroid gland anaplastic carcinoma visual epilepsy
622	3-hydroxybutyrate dehydrogenase 1	BDH1 Aliases: SDR9C1 short chain dehydrogenase/reductase family 9C, member 1	Homo sapiens (human)	COVID-19 Graves' disease X-linked dilated cardiomyopathy breast cancer cancer central nervous system cancer congestive heart failure dilated cardiomyopathy 1A 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 gliosarcoma hepatitis high grade glioma hyperthyroidism mixed glioma nicotine dependence thyrotoxicosis
669	bisphosphoglycerate mutase	BPGM	Homo sapiens (human)	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 familial erythrocytosis 8 normocytic anemia polycythemia vera polycythemia stress polycythemia
670	biphenyl hydrolase like	BPHL Aliases: Bph-rp VACVase breast epithelial mucin-associated antigen valacyclovir hydrolase	Homo sapiens (human)	bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood leukemia childhood osteosarcoma colon carcinoma colorectal cancer embryoma leukemia lung benign neoplasm lung cancer lung carcinoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
673	B-Raf proto-oncogene, serine/threonine kinase	BRAF	Homo sapiens (human)	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma
680	bombesin receptor subtype 3	BRS3	Homo sapiens (human)
683	bone marrow stromal cell antigen 1	BST1 Aliases: ADP-ribosyl cyclase 2 BST-1 CD157 NAD(+) nucleosidase cADPR2 cyclic ADP-ribose hydrolase	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 Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome acute monocytic leukemia acute myeloid leukemia allergic asthma asthma autism spectrum disorder autistic disorder benign mesothelioma benign pleural mesothelioma bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic lymphocytic leukemia depressive disorder dysthymic disorder embryoma essential hypertension hypertension inflammatory and toxic neuropathy intrinsic asthma lung benign neoplasm lung cancer lung carcinoma lung disease major depressive disorder malignant mesothelioma malignant pleural mesothelioma melancholic depression neurotic disorder obsolete melancholia ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural tuberculosis pneumonia prion disease prostate cancer prostate carcinoma tuberculosis
684	bone marrow stromal cell antigen 2	BST2 Aliases: BST-2 CD317 HM1.24 antiviral factor tetherin tetherin	Homo sapiens (human)	Burkitt lymphoma Down syndrome Ebola hemorrhagic fever Japanese encephalitis Sjogren's syndrome acquired immunodeficiency syndrome alternating hemiplegia of childhood anaplastic astrocytoma angioedema arthritis arthropathy autonomic neuropathy bladder carcinoma brain cancer breast cancer breast carcinoma cancer central nervous system disease chikungunya childhood cerebral astrocytoma childhood leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma conduct disorder dengue disease dengue hemorrhagic fever embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma exanthem fibrillary astrocytoma gemistocytic astrocytoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease influenza juvenile pilocytic astrocytoma kwashiorkor large intestine cancer leukemia liver cancer lupus erythematosus malignant astrocytoma marasmus melanoma multiple myeloma multiple sclerosis nasopharynx carcinoma nervous system disease nonpapillary renal cell carcinoma nutrition disease oral squamous cell carcinoma osteoarthritis papillary renal cell carcinoma parapsoriasis peeling skin syndrome pilocytic astrocytoma primary immunodeficiency disease protein-energy malnutrition protoplasmic astrocytoma psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scleroderma severe acute respiratory syndrome skin disease skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus systemic scleroderma transitional cell carcinoma urinary bladder cancer urticaria uterine corpus cancer viral infectious disease yellow fever
762	carbonic anhydrase 4	CA4 Aliases: CAIV Car4	Homo sapiens (human)	Behcet's disease Zollinger-Ellison syndrome achromatopsia acquired color blindness blindness blue color blindness brain cancer cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus large intestine cancer learning disability lung cancer lung non-small cell carcinoma myocarditis night blindness nonpapillary renal cell carcinoma obesity obsolete asthenopia ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus red color blindness red-green color blindness renal carcinoma renal cell carcinoma retinitis pigmentosa 17 retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 Aliases: alpha2delta-1 lncRNA-N3	Homo sapiens (human)	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 West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma

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