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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 **422001 - 422025** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
1212	clathrin light chain B	CLTB	Homo sapiens (human)
1211	clathrin light chain A	CLTA	Homo sapiens (human)
1209	CLPTM1 regulator of GABA type A receptor forward trafficking	CLPTM1	Homo sapiens (human)
1207	chloride nucleotide-sensitive channel 1A	CLNS1A	Homo sapiens (human)
1203	CLN5 intracellular trafficking protein	CLN5	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 Lafora disease MERRF syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome agnosia blepharospasm blindness brain disease cerebellar ataxia cerebellar disease cerebral degeneration early myoclonic encephalopathy epilepsy eye disease focal hand dystonia intellectual disability learning disability neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis retinal degeneration visual epilepsy
1201	CLN3 lysosomal/endosomal transmembrane protein, battenin	CLN3	Homo sapiens (human)
1200	tripeptidyl peptidase 1	TPP1	Homo sapiens (human)
1195	CDC like kinase 1	CLK1	Homo sapiens (human)
1192	chloride intracellular channel 1	CLIC1	Homo sapiens (human)
1191	clusterin	CLU	Homo sapiens (human)
1188	chloride voltage-gated channel Kb	CLCNKB	Homo sapiens (human)
1185	chloride voltage-gated channel 6	CLCN6	Homo sapiens (human)
1184	chloride voltage-gated channel 5	CLCN5	Homo sapiens (human)
1182	chloride voltage-gated channel 3	CLCN3	Homo sapiens (human)
1181	chloride voltage-gated channel 2	CLCN2	Homo sapiens (human)
1179	chloride channel accessory 1	CLCA1	Homo sapiens (human)
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)	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 Dent disease Pick's disease Reye syndrome acute myeloid leukemia allergic asthma allergic rhinitis arthritis arthropathy asthma autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 blindness cancer celiac disease central nervous system cancer cerebral degeneration chronic ethmoiditis chronic sphenoidal sinusitis colorectal cancer colorectal carcinoma corneal disease craniosynostosis embryoma eosinophilic esophagitis epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis gliosarcoma glomerulonephritis high grade glioma hypertension immune system disease intrinsic asthma islet cell tumor keratoconus kidney disease large intestine cancer male infertility mixed glioma myasthenia gravis myotonia congenita nasopharynx carcinoma nephritis nephrolithiasis nephrosis osteoarthritis osteopetrosis osteoporosis osteosclerosis parapsoriasis psoriasis pustulosis of palm and sole pyoureter thyroid gland anaplastic carcinoma uric acid nephrolithiasis vasomotor rhinitis
1173	adaptor related protein complex 2 subunit mu 1	AP2M1	Homo sapiens (human)
1159	creatine kinase, mitochondrial 1B	CKMT1B	Homo sapiens (human)
1147	component of inhibitor of nuclear factor kappa B kinase complex	CHUK	Homo sapiens (human)
1146	cholinergic receptor nicotinic gamma subunit	CHRNG	Homo sapiens (human)
1145	cholinergic receptor nicotinic epsilon subunit	CHRNE	Homo sapiens (human)
1144	cholinergic receptor nicotinic delta subunit	CHRND	Homo sapiens (human)
1143	cholinergic receptor nicotinic beta 4 subunit	CHRNB4	Homo sapiens (human)
1142	cholinergic receptor nicotinic beta 3 subunit	CHRNB3	Homo sapiens (human)

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