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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 **15676 - 15700** of **393515** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
112962530	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Apteryx rowi (Okarito brown kiwi)
103002161	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Balaenoptera acutorostrata (minke whale)
106978342	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Acinonyx jubatus (cheetah)
105289362	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Pteropus vampyrus (large flying fox)
106552084	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Thamnophis sirtalis
104327569	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Opisthocomus hoazin
113448604	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Pseudonaja textilis
125701838	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Lagopus muta (rock ptarmigan)
120988628	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Bufo bufo (common toad)
117672183	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Pantherophis guttatus
110471786	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Lonchura striata domestica (Bengalese finch)
102434782	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Myotis lucifugus (little brown bat)
111538596	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Piliocolobus tephrosceles (Ugandan red Colobus)
102066029	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Zonotrichia albicollis (white-throated sparrow)
102449675	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Pelodiscus sinensis (Chinese soft-shelled turtle)
118655501	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Myotis myotis
113486147	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Athene cunicularia (burrowing owl)
101806637	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Ficedula albicollis (Collared flycatcher)
102739310	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Leptonychotes weddellii (Weddell seal)
120934673	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Rana temporaria (common frog)
120509688	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Passer montanus (Eurasian tree sparrow)
116738763	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Phocoena sinus (vaquita)
102089604	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Columba livia (rock pigeon)
23545	ATPase H+ transporting V0 subunit a2	ATP6V0A2 Aliases: ATP6N1D ATP6a2 J6B7 RTF Stv1 TJ6 TJ6M TJ6s V-ATPase subunit a2 V-type proton ATPase 116 kDa subunit a2 Vph1 a2 a2V infantile malignant osteopetrosis regeneration and tolerance factor	Homo sapiens (human)	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 autosomal recessive osteopetrosis 1 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il 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 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease wrinkly skin syndrome
116228641	ATPase H+ transporting V0 subunit a2	ATP6V0A2	Phasianus colchicus (Ring-necked pheasant)

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