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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 **8701 - 8725** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
288	ankyrin 3	ANK3	Homo sapiens (human)
255043	transmembrane protein 86B	TMEM86B Aliases: MGC30208 alkenylglycerophosphocholine hydrolase alkenylglycerophosphoethanolamine hydrolase	Homo sapiens (human)
7469	negative elongation factor complex member A	NELFA	Homo sapiens (human)
7913	DEK proto-oncogene	DEK	Homo sapiens (human)
6326	sodium voltage-gated channel alpha subunit 2	SCN2A	Homo sapiens (human)
2219	ficolin 1	FCN1 Aliases: FCNM	Homo sapiens (human)	Clostridium difficile colitis Kawasaki disease acute myocardial infarction arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome brain ischemia brain stem infarction cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chronic fatigue syndrome colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cystic fibrosis embryoma encephalomyelitis familial hyperlipidemia immune system disease large intestine cancer lepromatous leprosy leprosy lupus nephritis myocardial infarction perinatal necrotizing enterocolitis rheumatic fever rheumatoid arthritis silent myocardial infarction transient cerebral ischemia vasculitis vertebrobasilar insufficiency
29095	ORMDL sphingolipid biosynthesis regulator 2	ORMDL2 Aliases: HSPC160 MST095 MSTP095 adoplin-2	Homo sapiens (human)	allergic asthma asthma intrinsic asthma
85456	tankyrase 1 binding protein 1	TNKS1BP1	Homo sapiens (human)
81448	olfactory receptor family 6 subfamily K member 2	OR6K2	Homo sapiens (human)
999	cadherin 1	CDH1	Homo sapiens (human)
79796	ALG9 alpha-1,2-mannosyltransferase	ALG9 Aliases: dol-P-Man dependent alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	Homo sapiens (human)	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
219790	rhotekin 2	RTKN2	Homo sapiens (human)
91452	acyl-CoA binding domain containing 5	ACBD5	Homo sapiens (human)
608	TNF receptor superfamily member 17	TNFRSF17	Homo sapiens (human)
255738	proprotein convertase subtilisin/kexin type 9	PCSK9	Homo sapiens (human)
114799	establishment of sister chromatid cohesion N-acetyltransferase 1	ESCO1	Homo sapiens (human)
26658	olfactory receptor family 7 subfamily C member 2	OR7C2	Homo sapiens (human)
8737	receptor interacting serine/threonine kinase 1	RIPK1	Homo sapiens (human)
85379	KIAA1671	KIAA1671	Homo sapiens (human)
9788	MTSS I-BAR domain containing 1	MTSS1	Homo sapiens (human)
113146	AHNAK nucleoprotein 2	AHNAK2	Homo sapiens (human)
9289	adhesion G protein-coupled receptor G1	ADGRG1	Homo sapiens (human)
11096	ADAM metallopeptidase with thrombospondin type 1 motif 5	ADAMTS5	Homo sapiens (human)
29929	ALG6 alpha-1,3-glucosyltransferase	ALG6 Aliases: dolichyl-P-Glc:Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	Homo sapiens (human)	antithrombin III deficiency congenital disorder of glycosylation Ia congenital disorder of glycosylation Ic congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia mechanical strabismus ophthalmoplegia protein C deficiency protein S deficiency strabismus thrombophilia visual epilepsy
6578	solute carrier organic anion transporter family member 2A1	SLCO2A1	Homo sapiens (human)

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