GlyCosmos Portal

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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 **7451 - 7475** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
3934	lipocalin 2	LCN2	Homo sapiens (human)
83480	pseudouridine synthase 3	PUS3	Homo sapiens (human)
9468	phosphate cytidylyltransferase 1B, choline	PCYT1B Aliases: CCT-beta CCTbeta CTB CTP:phosphocholine cytidylyltransferase-beta choline-phosphate cytidylyltransferase beta phosphorylcholine transferase beta	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 Clouston syndrome Leber congenital amaurosis 1 Pick's disease Reye syndrome adult respiratory distress syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma breast ductal carcinoma cancer cerebral degeneration cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis large intestine cancer liver cancer liver carcinoma newborn respiratory distress syndrome progressive muscular atrophy prostate cancer prostate carcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis
22820	COPI coat complex subunit gamma 1	COPG1	Homo sapiens (human)
79693	yrdC N6-threonylcarbamoyltransferase domain containing	YRDC	Homo sapiens (human)
3559	interleukin 2 receptor subunit alpha	IL2RA	Homo sapiens (human)
10004	N-acetylated alpha-linked acidic dipeptidase like 1	NAALADL1	Homo sapiens (human)
9793	cytoskeleton associated protein 5	CKAP5	Homo sapiens (human)
133584	EGF like, fibronectin type III and laminin G domains	EGFLAM	Homo sapiens (human)
11009	interleukin 24	IL24	Homo sapiens (human)
256223	CMT1A duplicated region transcript 15 like 2	CDRT15L2	Homo sapiens (human)
51729	WW domain binding protein 11	WBP11	Homo sapiens (human)
50649	Rho guanine nucleotide exchange factor 4	ARHGEF4	Homo sapiens (human)
3760	potassium inwardly rectifying channel subfamily J member 3	KCNJ3	Homo sapiens (human)
64788	lipase maturation factor 1	LMF1	Homo sapiens (human)
56100	protocadherin gamma subfamily B, 6	PCDHGB6	Homo sapiens (human)
5675	pregnancy specific beta-1-glycoprotein 6	PSG6	Homo sapiens (human)
10003	N-acetylated alpha-linked acidic dipeptidase 2	NAALAD2	Homo sapiens (human)
5880	Rac family small GTPase 2	RAC2	Homo sapiens (human)
10802	SEC24 homolog A, COPII coat complex component	SEC24A	Homo sapiens (human)
51102	mitochondrial trans-2-enoyl-CoA reductase	MECR Aliases: CGI-63 ETR1 FASN2B NRBF1 mitochondrial 2-enoyl thioester reductase nuclear receptor binding factor 1	Homo sapiens (human)	Leber hereditary optic neuropathy with demyelinating disease of CNS Unverricht-Lundborg syndrome blepharospasm blindness cerebral palsy childhood-onset dystonia with optic atrophy and basal ganglia abnormalities choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus disorder of sexual development dissociated nystagmus dystonia early myoclonic encephalopathy focal hand dystonia generalized dystonia hemiplegia hermaphroditism large intestine cancer lingual-facial-buccal dyskinesia optic atrophy pathologic nystagmus pseudohermaphroditism schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus syndromic X-linked intellectual disability type 10
55937	apolipoprotein M	APOM	Homo sapiens (human)
113730	kelch domain containing 7B	KLHDC7B	Homo sapiens (human)
89801	protein phosphatase 1 regulatory subunit 3F	PPP1R3F	Homo sapiens (human)
50834	taste 2 receptor member 1	TAS2R1	Homo sapiens (human)

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