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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 **251 - 275** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
481	ATPase Na+/K+ transporting subunit beta 1	ATP1B1	Homo sapiens (human)	essential hypertension
482	ATPase Na+/K+ transporting subunit beta 2	ATP1B2	Homo sapiens (human)
483	ATPase Na+/K+ transporting subunit beta 3	ATP1B3	Homo sapiens (human)
488	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	ATP2A2	Homo sapiens (human)	acrokeratosis verruciformis essential hypertension keratosis follicularis pulmonary hypertension
489	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3	ATP2A3	Homo sapiens (human)
493	ATPase plasma membrane Ca2+ transporting 4	ATP2B4	Homo sapiens (human)
496	ATPase H+/K+ transporting subunit beta	ATP4B	Homo sapiens (human)	atrophic gastritis autoimmune gastritis stomach cancer
498	ATP synthase F1 subunit alpha	ATP5F1A	Homo sapiens (human)	combined oxidative phosphorylation deficiency 22 mitochondrial complex V (ATP synthase) deficiency nuclear type 4A mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
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)	early-onset vitamin B6-dependent epilepsy 4
506	ATP synthase F1 subunit beta	ATP5F1B	Homo sapiens (human)
509	ATP synthase F1 subunit gamma	ATP5F1C	Homo sapiens (human)
521	ATP synthase membrane subunit e	ATP5ME	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)	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
527	ATPase H+ transporting V0 subunit c	ATP6V0C	Homo sapiens (human)	early-onset epilepsy 3 thyroid gland carcinoma
529	ATPase H+ transporting V1 subunit E1	ATP6V1E1	Homo sapiens (human)	autosomal recessive cutis laxa type IIC
535	ATPase H+ transporting V0 subunit a1	ATP6V0A1	Homo sapiens (human)	developmental and epileptic encephalopathy 104
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)	immunodeficiency 47
538	ATPase copper transporting alpha	ATP7A	Homo sapiens (human)	Menkes disease X-linked distal spinal muscular atrophy 3 cutis laxa occipital horn syndrome
540	ATPase copper transporting beta	ATP7B	Homo sapiens (human)	Wilson disease
545	ATR serine/threonine kinase	ATR	Homo sapiens (human)	Seckel syndrome 1 adenoid cystic carcinoma colon cancer lung cancer pancreatic cancer
546	ATRX chromatin remodeler	ATRX	Homo sapiens (human)	X-linked mental retardation-hypotonic facies syndrome-1 alpha thalassemia-X-linked intellectual disability syndrome alpha-thalassemia myelodysplasia syndrome high grade glioma lung small cell carcinoma
551	arginine vasopressin	AVP	Homo sapiens (human)	diabetes insipidus neurohypophyseal diabetes insipidus
552	arginine vasopressin receptor 1A	AVPR1A	Homo sapiens (human)	hypertension
553	arginine vasopressin receptor 1B	AVPR1B	Homo sapiens (human)	autism spectrum disorder bipolar disorder mood disorder
554	arginine vasopressin receptor 2	AVPR2	Homo sapiens (human)	X-linked nephrogenic diabetes insipidus nephrogenic diabetes insipidus nephrogenic syndrome of inappropriate antidiuresis

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