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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	October 29, 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 **9726 - 9750** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
529	ATPase H+ transporting V1 subunit E1	ATP6V1E1	Homo sapiens (human)
527	ATPase H+ transporting V0 subunit c	ATP6V0C	Homo sapiens (human)
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
521	ATP synthase membrane subunit e	ATP5ME	Homo sapiens (human)
509	ATP synthase F1 subunit gamma	ATP5F1C	Homo sapiens (human)
506	ATP synthase F1 subunit beta	ATP5F1B	Homo sapiens (human)
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
498	ATP synthase F1 subunit alpha	ATP5F1A	Homo sapiens (human)
496	ATPase H+/K+ transporting subunit beta	ATP4B	Homo sapiens (human)
493	ATPase plasma membrane Ca2+ transporting 4	ATP2B4	Homo sapiens (human)
489	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3	ATP2A3	Homo sapiens (human)
483	ATPase Na+/K+ transporting subunit beta 3	ATP1B3	Homo sapiens (human)
482	ATPase Na+/K+ transporting subunit beta 2	ATP1B2	Homo sapiens (human)
481	ATPase Na+/K+ transporting subunit beta 1	ATP1B1	Homo sapiens (human)
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
476	ATPase Na+/K+ transporting subunit alpha 1	ATP1A1	Homo sapiens (human)
473	arginine-glutamic acid dipeptide repeats	RERE	Homo sapiens (human)
472	ATM serine/threonine kinase	ATM	Homo sapiens (human)
471	5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase	ATIC Aliases: AICARFT IMPCHASE PURH phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Homo sapiens (human)
468	activating transcription factor 4	ATF4	Homo sapiens (human)	borna disease prostate carcinoma pulmonary venoocclusive disease
467	activating transcription factor 3	ATF3	Homo sapiens (human)	prostate cancer pulmonary tuberculosis
466	activating transcription factor 1	ATF1	Homo sapiens (human)
463	zinc finger homeobox 3	ZFHX3	Homo sapiens (human)
462	serpin family C member 1	SERPINC1	Homo sapiens (human)
460	astrotactin 1	ASTN1	Homo sapiens (human)

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