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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 **826 - 850** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
1781	dynein cytoplasmic 1 intermediate chain 2	DYNC1I2	Homo sapiens (human)
1783	dynein cytoplasmic 1 light intermediate chain 2	DYNC1LI2	Homo sapiens (human)
1785	dynamin 2	DNM2 Aliases: CMT2M CMTDI1 CMTDIB DI-CMTB DYN2 DYNII cytoskeletal protein dynamin II	Homo sapiens (human)	Charcot-Marie-Tooth disease dominant intermediate B centronuclear myopathy 1 lethal congenital contracture syndrome
1786	DNA methyltransferase 1	DNMT1	Homo sapiens (human)	Graves' disease autosomal dominant cerebellar ataxia, deafness and narcolepsy hereditary sensory neuropathy type 1E hereditary sensory neuropathy lung non-small cell carcinoma
1793	dedicator of cytokinesis 1	DOCK1	Homo sapiens (human)
1795	dedicator of cytokinesis 3	DOCK3	Homo sapiens (human)	attention deficit hyperactivity disorder
1798	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	DPAGT1 Aliases: ALG7 CDG-Ij D11S366 DGPT GPT GlcNAc-1-P transferase 1 UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Homo sapiens (human)	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
1800	dipeptidase 1	DPEP1	Homo sapiens (human)	hepatoblastoma
1802	diphthamide biosynthesis 2	DPH2	Homo sapiens (human)	diphthamide deficiency syndrome 2
1803	dipeptidyl peptidase 4	DPP4	Homo sapiens (human)	Middle East respiratory syndrome type 2 diabetes mellitus
1804	dipeptidyl peptidase like 6	DPP6	Homo sapiens (human)	amyotrophic lateral sclerosis autosomal dominant intellectual developmental disorder 33 spinal muscular atrophy
1806	dihydropyrimidine dehydrogenase	DPYD	Homo sapiens (human)	acute lymphoblastic leukemia dihydropyrimidine dehydrogenase deficiency pancreatic cancer
1808	dihydropyrimidinase like 2	DPYSL2	Homo sapiens (human)
1809	dihydropyrimidinase like 3	DPYSL3	Homo sapiens (human)
1811	solute carrier family 26 member 3	SLC26A3	Homo sapiens (human)	congenital secretory chloride diarrhea 1 diarrhea
1812	dopamine receptor D1	DRD1	Homo sapiens (human)	hypertension kidney failure
1813	dopamine receptor D2	DRD2	Homo sapiens (human)	alcohol dependence alcohol-induced mental disorder anxiety disorder cocaine dependence depressive disorder end stage renal disease heroin dependence hypertension migraine with aura movement disease nicotine dependence obesity opiate dependence type 2 diabetes mellitus
1814	dopamine receptor D3	DRD3	Homo sapiens (human)	essential tremor 1 essential tremor schizophrenia
1815	dopamine receptor D4	DRD4	Homo sapiens (human)	Gilles de la Tourette syndrome alcohol use disorder antisocial personality disorder attention deficit hyperactivity disorder cannabis abuse conduct disorder dyslexia heroin dependence intellectual disability liver cirrhosis nicotine dependence opioid abuse pathological gambling substance abuse
1816	dopamine receptor D5	DRD5	Homo sapiens (human)	attention deficit hyperactivity disorder blepharospasm
1820	AT-rich interaction domain 3A	ARID3A	Homo sapiens (human)
1821	dystrophin related protein 2	DRP2	Homo sapiens (human)
1822	atrophin 1	ATN1	Homo sapiens (human)	dentatorubral-pallidoluysian atrophy schizophrenia
1823	desmocollin 1	DSC1	Homo sapiens (human)
1824	desmocollin 2	DSC2	Homo sapiens (human)	arrhythmogenic right ventricular cardiomyopathy arrhythmogenic right ventricular dysplasia 11

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