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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
GlycoGene Database (GGDB)
KEGG GENES Database	September 20, 2023
Plant GARDEN
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 **15851 - 15875** of **393515** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
113918902	ATPase H+ transporting V1 subunit A	ATP6V1A	Zalophus californianus (California sea lion)
120400535	ATPase H+ transporting V1 subunit A	ATP6V1A	Mauremys reevesii (Reeves's turtle)
104514022	ATPase H+ transporting V1 subunit A	ATP6V1A	Eurypyga helias (sunbittern)
120994374	ATPase H+ transporting V1 subunit A	ATP6V1A	Bufo bufo (common toad)
102038391	ATPase H+ transporting V1 subunit A	ATP6V1A	Geospiza fortis (medium ground-finch)
123827197	ATPase H+ transporting V1 subunit A	ATP6V1A	Phyllostomus hastatus (greater spear-nosed bat)
117036068	ATPase H+ transporting V1 subunit A	ATP6V1A	Rhinolophus ferrumequinum (greater horseshoe bat)
106829494	ATPase H+ transporting V1 subunit A	ATP6V1A	Equus asinus (ass)
104280460	ATPase H+ transporting V1 subunit A	ATP6V1A	Apaloderma vittatum (bar-tailed trogon)
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
118676142	ATPase H+ transporting V1 subunit A	ATP6V1A	Myotis myotis
104252747	ATPase H+ transporting V1 subunit A	ATP6V1A	Gavia stellata (red-throated loon)
103678812	ATPase H+ transporting V1 subunit A	ATP6V1A	Ursus maritimus (polar bear)
102128783	ATPase H+ transporting V1 subunit A	ATP6V1A	Macaca fascicularis (crab-eating macaque)
123239493	ATPase H+ transporting V1 subunit A	ATP6V1A	Gracilinanus agilis (Agile Gracile Mouse Opossum)
104541713	ATPase H+ transporting V1 subunit A	ATP6V1A	Mesitornis unicolor (brown roatelo)
112965950	ATPase H+ transporting V1 subunit A	ATP6V1A	Apteryx rowi (Okarito brown kiwi)
112849312	ATPase H+ transporting V1 subunit A	ATP6V1A	Puma concolor (puma)
102736081	ATPase H+ transporting V1 subunit A	ATP6V1A	Leptonychotes weddellii (Weddell seal)
104356646	ATPase H+ transporting V1 subunit A	ATP6V1A	Tyto alba (common barn owl)
116955892	ATPase H+ transporting V1 subunit A	ATP6V1A	Petromyzon marinus (sea lamprey)
108396238	ATPase H+ transporting V1 subunit A	ATP6V1A	Manis javanica (Malayan pangolin)
113477758	ATPase H+ transporting V1 subunit A	ATP6V1A	Athene cunicularia (burrowing owl)
106497259	ATPase H+ transporting V1 subunit A	ATP6V1A	Apteryx mantelli mantelli
125622008	ATPase H+ transporting V1 subunit A	ATP6V1A	Caretta caretta (Loggerhead turtle)

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