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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 **2626 - 2650** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
200185	keratinocyte associated protein 2	KRTCAP2 Aliases: KCP2	Homo sapiens (human)
200186	CREB regulated transcription coactivator 2	CRTC2	Homo sapiens (human)	type 2 diabetes mellitus
200576	phosphoinositide kinase, FYVE-type zinc finger containing	PIKFYVE Aliases: FAB1 KIAA0981 MGC40423 PIP5K ZFYVE29 p235 zinc finger, FYVE domain containing 29	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 B-cell lymphoma Crohn's colitis Crohn's disease Fleck corneal dystrophy Pick's disease Reye syndrome breast cancer cancer cardiomyopathy cerebral degeneration embryoma endomyocardial fibrosis gestational diabetes hypertrophic cardiomyopathy legionellosis multiple myeloma obsolete asthenopia obsolete ymphosarcoma pneumonia transitional cell carcinoma
201562	3-hydroxyacyl-CoA dehydratase 2	HACD2 Aliases: Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	Homo sapiens (human)	cancer
201595	STT3 oligosaccharyltransferase complex catalytic subunit B	STT3B Aliases: Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B FLJ90106 SIMP STT3-B dolichyl-diphosphooligosaccharide protein glycotransferase source of immunodominant MHC associated peptides	Homo sapiens (human)	Japanese encephalitis congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix congenital disorder of glycosylation cryptorchidism dengue disease epilepsy intellectual disability learning disability microcephaly optic atrophy placental insufficiency sleeping sickness thrombocytopenia trypanosomiasis viral infectious disease visual epilepsy yellow fever
204219	ceramide synthase 3	CERS3 Aliases: MGC27091	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome Weill-Marchesani syndrome achondroplasia acrodermatitis alopecia anhidrosis atopic dermatitis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis dermatitis ectropion hypohidrosis ichthyosis keratitis keratoconjunctivitis keratosis follicularis mongolian spot nonepidermolytic palmoplantar keratoderma obsolete congenital ichthyosiform erythroderma palmoplantar keratosis pseudoxanthoma elasticum sensorineural hearing loss
207839	polypeptide N-acetylgalactosaminyltransferase 6	Galnt6	Mus musculus (house mouse)
207958	ALG11 alpha-1,2-mannosyltransferase	Alg11	Mus musculus (house mouse)	congenital disorder of glycosylation Ip
208211	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	Mus musculus (house mouse)	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
208624	ALG3 alpha-1,3- mannosyltransferase	Alg3	Mus musculus (house mouse)	congenital disorder of glycosylation Id congenital disorder of glycosylation
209692	dehydrogenase E1 and transketolase domain containing 1	Dhtkd1	Mus musculus (house mouse)	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
210004	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1	B3gntl1	Mus musculus (house mouse)
210808	laccase domain containing 1	Lacc1	Mus musculus (house mouse)	juvenile rheumatoid arthritis
210973	kelch repeat and BTB (POZ) domain containing 2	Kbtbd2	Mus musculus (house mouse)
211286	ceroid-lipofuscinosis, neuronal 5	Cln5	Mus musculus (house mouse)	neuronal ceroid lipofuscinosis 5
212032	hexokinase 3	Hk3	Mus musculus (house mouse)	glucose metabolism disease
212974	protein glucosylgalactosylhydroxylysine glucosidase	Pgghg	Mus musculus (house mouse)
212996	polypeptide N-acetylgalactosaminyltransferase 17	Galnt17	Mus musculus (house mouse)
213012	abhydrolase domain containing 10	Abhd10	Mus musculus (house mouse)
213053	solute carrier family 39 (zinc transporter), member 14	Slc39a14	Mus musculus (house mouse)	hypermanganesemia with dystonia 2
213819	CAS1 domain containing 1	Casd1	Mus musculus (house mouse)
214424	poly (ADP-ribose) polymerase family, member 16	Parp16	Mus musculus (house mouse)
214505	N-acetylglucosamine-1-phosphotransferase, gamma subunit	Gnptg	Mus musculus (house mouse)	glycoproteinosis mucolipidosis III gamma
215090	mannosidase, endo-alpha-like	Maneal	Mus musculus (house mouse)
215493	alpha 1,3-galactosyltransferase 2	A3galt2	Mus musculus (house mouse)

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