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 **176 - 200** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
1870	E2F transcription factor 2	E2F2	Homo sapiens (human)
122970	acyl-CoA thioesterase 4	ACOT4 Aliases: FLJ31235 PTE-Ib PTE2B	Homo sapiens (human)	cerebral infarction cerebrovascular disease
23621	beta-secretase 1	BACE1	Homo sapiens (human)
3000	guanylate cyclase 2D, retinal	GUCY2D	Homo sapiens (human)
9144	synaptogyrin 2	SYNGR2	Homo sapiens (human)
9524	trans-2,3-enoyl-CoA reductase	TECR Aliases: MRT14 TER very-long-chain enoyl-CoA reductase	Homo sapiens (human)	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
130752	malate dehydrogenase 1B	MDH1B	Homo sapiens (human)
9479	mitogen-activated protein kinase 8 interacting protein 1	MAPK8IP1	Homo sapiens (human)
6949	treacle ribosome biogenesis factor 1	TCOF1	Homo sapiens (human)
988	cell division cycle 5 like	CDC5L	Homo sapiens (human)
6880	TATA-box binding protein associated factor 9	TAF9	Homo sapiens (human)
8773	synaptosome associated protein 23	SNAP23	Homo sapiens (human)
120103	solute carrier family 36 member 4	SLC36A4	Homo sapiens (human)
81849	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5	ST6GALNAC5 Aliases: MGC3184 ST6GalNAcV	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ coronary artery disease embryoma gliosarcoma high grade glioma lymphoma mixed glioma nutmeg liver obsolete ymphosarcoma rheumatoid arthritis
8796	sciellin	SCEL	Homo sapiens (human)
84171	lysyl oxidase like 4	LOXL4	Homo sapiens (human)
4588	mucin 6, oligomeric mucus/gel-forming (gene/pseudogene)	MUC6	Homo sapiens (human)
58513	epidermal growth factor receptor pathway substrate 15 like 1	EPS15L1	Homo sapiens (human)
6727	signal recognition particle 14	SRP14	Homo sapiens (human)
7040	transforming growth factor beta 1	TGFB1	Homo sapiens (human)
1137	cholinergic receptor nicotinic alpha 4 subunit	CHRNA4	Homo sapiens (human)
9425	chromodomain Y like	CDYL	Homo sapiens (human)
5727	patched 1	PTCH1	Homo sapiens (human)
285590	SH3 and PX domains 2B	SH3PXD2B	Homo sapiens (human)
10803	C-C motif chemokine receptor 9	CCR9	Homo sapiens (human)

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