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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 **7226 - 7250** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
35	acyl-CoA dehydrogenase short chain	ACADS Aliases: ACAD3 SCAD	Homo sapiens (human)	Bell's palsy Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Stevens-Johnson syndrome X-linked Aarskog syndrome alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bipolar disorder cancer cardiomyopathy chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease congestive heart failure coronary artery disease embryoma endomyocardial fibrosis epilepsy erythema multiforme facial nerve disease facial paralysis familial periodic paralysis hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer medium chain acyl-CoA dehydrogenase deficiency microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myopathy nutmeg liver pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scoliosis short chain acyl-CoA dehydrogenase deficiency visual epilepsy
50801	potassium two pore domain channel subfamily K member 4	KCNK4	Homo sapiens (human)
126014	osteoclast associated Ig-like receptor	OSCAR	Homo sapiens (human)
10361	nucleophosmin/nucleoplasmin 2	NPM2	Homo sapiens (human)
146059	codanin 1	CDAN1	Homo sapiens (human)
441381	leucine rich repeat containing 24	LRRC24	Homo sapiens (human)
29766	tropomodulin 3	TMOD3	Homo sapiens (human)
57502	neuroligin 4 X-linked	NLGN4X	Homo sapiens (human)
10497	unc-13 homolog B	UNC13B	Homo sapiens (human)
123	perilipin 2	PLIN2	Homo sapiens (human)
11016	activating transcription factor 7	ATF7	Homo sapiens (human)
3845	KRAS proto-oncogene, GTPase	KRAS Aliases: K-Ras4B KRAS1	Homo sapiens (human)
80243	phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2	PREX2	Homo sapiens (human)
23387	SIK family kinase 3	SIK3	Homo sapiens (human)
140687	glucosaminyl (N-acetyl) transferase family member 7	GCNT7 Aliases: dJ1153D9.2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
10672	G protein subunit alpha 13	GNA13	Homo sapiens (human)
10040	target of myb1 like 1 membrane trafficking protein	TOM1L1	Homo sapiens (human)
9175	mitogen-activated protein kinase kinase kinase 13	MAP3K13	Homo sapiens (human)
128646	signal regulatory protein delta	SIRPD	Homo sapiens (human)
2903	glutamate ionotropic receptor NMDA type subunit 2A	GRIN2A	Homo sapiens (human)
79071	ELOVL fatty acid elongase 6	ELOVL6 Aliases: FLJ23378 LCE MGC5487	Homo sapiens (human)	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
1241	leukotriene B4 receptor	LTB4R	Homo sapiens (human)
25907	transmembrane protein 158	TMEM158	Homo sapiens (human)
23087	tripartite motif containing 35	TRIM35	Homo sapiens (human)
27344	proprotein convertase subtilisin/kexin type 1 inhibitor	PCSK1N	Homo sapiens (human)

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