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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 **576 - 600** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
1147	component of inhibitor of nuclear factor kappa B kinase complex	CHUK	Homo sapiens (human)	fetal encasement syndrome liver cancer prostate cancer
1159	creatine kinase, mitochondrial 1B	CKMT1B	Homo sapiens (human)
1173	adaptor related protein complex 2 subunit mu 1	AP2M1	Homo sapiens (human)	autosomal dominant intellectual developmental disorder
1178	Charcot-Leyden crystal galectin	CLC Aliases: Gal-10 LGALS10 MGC149659 eosinophil lysophospholipase galectin 10 lectin, galactoside-binding, soluble, 10 lysolecithin acylhydrolase	Homo sapiens (human)
1179	chloride channel accessory 1	CLCA1	Homo sapiens (human)	asthma chronic obstructive pulmonary disease
1181	chloride voltage-gated channel 2	CLCN2	Homo sapiens (human)	obsolete idiopathic generalized epilepsy 11 primary hyperaldosteronism
1182	chloride voltage-gated channel 3	CLCN3	Homo sapiens (human)
1184	chloride voltage-gated channel 5	CLCN5	Homo sapiens (human)	Dent disease 1 X-linked nephrolithiasis type I X-linked recessive hypophosphatemic rickets low molecular weight proteinuria with hypercalciuric nephrocalcinosis
1185	chloride voltage-gated channel 6	CLCN6	Homo sapiens (human)	coronary artery disease
1188	chloride voltage-gated channel Kb	CLCNKB	Homo sapiens (human)	Bartter disease type 3 Bartter disease type 4b Gitelman syndrome hypertension
1191	clusterin	CLU	Homo sapiens (human)	atherosclerosis breast cancer diabetic retinopathy exfoliation syndrome hypertension inclusion body myositis muscular disease myocardial infarction pre-eclampsia
1192	chloride intracellular channel 1	CLIC1	Homo sapiens (human)
1195	CDC like kinase 1	CLK1	Homo sapiens (human)
1200	tripeptidyl peptidase 1	TPP1	Homo sapiens (human)	autosomal recessive spinocerebellar ataxia 7 neuronal ceroid lipofuscinosis 2
1201	CLN3 lysosomal/endosomal transmembrane protein, battenin	CLN3	Homo sapiens (human)	neuronal ceroid lipofuscinosis 3
1203	CLN5 intracellular trafficking protein	CLN5	Homo sapiens (human)	neuronal ceroid lipofuscinosis 5
1207	chloride nucleotide-sensitive channel 1A	CLNS1A	Homo sapiens (human)
1209	CLPTM1 regulator of GABA type A receptor forward trafficking	CLPTM1	Homo sapiens (human)
1211	clathrin light chain A	CLTA	Homo sapiens (human)
1212	clathrin light chain B	CLTB	Homo sapiens (human)
1213	clathrin heavy chain	CLTC	Homo sapiens (human)	autosomal dominant intellectual developmental disorder 56
1215	chymase 1	CMA1	Homo sapiens (human)	asthma atopic dermatitis hypertrophic cardiomyopathy sarcoidosis
1230	C-C motif chemokine receptor 1	CCR1	Homo sapiens (human)	allergic contact dermatitis rheumatoid arthritis
1232	C-C motif chemokine receptor 3	CCR3	Homo sapiens (human)	asthma ovary epithelial cancer rhinitis
1233	C-C motif chemokine receptor 4	CCR4	Homo sapiens (human)

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