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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	July 8, 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 **1176 - 1200** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
108715547	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase	LOC108715547	Xenopus laevis (African clawed frog)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
393326	ST3 beta-galactoside alpha-2,3-sialyltransferase 3a	st3gal3a	Danio rerio (zebrafish)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
20441	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	Mus musculus (house mouse)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
407659	ST3 beta-galactoside alpha-2,3-sialyltransferase 3b	st3gal3b	Danio rerio (zebrafish)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
64445	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	Rattus norvegicus (Norway rat)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
402789	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	st3gal3	Xenopus tropicalis (tropical clawed frog)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15 retinitis pigmentosa 33 retinitis pigmentosa
39048	Tequila	teq	Drosophila melanogaster (fruit fly)	autosomal recessive intellectual developmental disorder 1 intellectual disability
141	ADP-ribosylarginine hydrolase	ADPRH Aliases: ARH1 [Protein ADP-ribosylarginine] hydrolase	Homo sapiens (human)	autosomal recessive hypercholesterolemia cancer cardiomyopathy cholera endomyocardial fibrosis familial hypercholesterolemia hypertrophic cardiomyopathy ovarian cancer ovarian carcinoma
54936	ADP-ribosylserine hydrolase	ADPRS Aliases: ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	Homo sapiens (human)	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
24788	sorbitol dehydrogenase	Sord	Rattus norvegicus (Norway rat)	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
853624	L-iditol 2-dehydrogenase SOR1	SOR1	Saccharomyces cerevisiae S288C	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
851351	L-iditol 2-dehydrogenase SOR2	SOR2	Saccharomyces cerevisiae S288C	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
20322	sorbitol dehydrogenase	Sord	Mus musculus (house mouse)	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
850759	D-xylulose reductase XYL2	XYL2	Saccharomyces cerevisiae S288C	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
407846	ST6 beta-galactosamide alpha-2,6-sialyltranferase 2	st6gal2	Xenopus tropicalis (tropical clawed frog)	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
855928	phosphatidylinositol N-acetylglucosaminyltransferase SPT14	SPT14	Saccharomyces cerevisiae S288C	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	Rattus norvegicus (Norway rat)	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	Danio rerio (zebrafish)	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
37020	Phosphatidylinositol glycan anchor biosynthesis class A	PIG-A	Drosophila melanogaster (fruit fly)	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	Mus musculus (house mouse)	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	Caenorhabditis elegans	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
100158632	phosphatidylinositol glycan anchor biosynthesis class A	piga	Xenopus tropicalis (tropical clawed frog)	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
280	amylase alpha 2B	AMY2B	Homo sapiens (human)	autosomal recessive congenital ichthyosis 1 ichthyosis keratosis follicularis lung benign neoplasm lung carcinoma mongolian spot obsolete congenital ichthyosiform erythroderma pseudoxanthoma elasticum
2135	exostosin like glycosyltransferase 2	EXTL2 Aliases: alpha-1,4-N-acteylhexosaminyltransferase	Homo sapiens (human)	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 Aliases: GALNAC-T8 polypeptide GalNAc transferase 8	Homo sapiens (human)	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C

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