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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 **390876 - 390900** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
211286	ceroid-lipofuscinosis, neuronal 5	Cln5	Mus musculus (house mouse)	neuronal ceroid lipofuscinosis 5
210973	kelch repeat and BTB (POZ) domain containing 2	Kbtbd2	Mus musculus (house mouse)
210808	laccase domain containing 1	Lacc1	Mus musculus (house mouse)	juvenile rheumatoid arthritis
210004	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1	B3gntl1	Mus musculus (house mouse)
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
208624	ALG3 alpha-1,3- mannosyltransferase	Alg3	Mus musculus (house mouse)	congenital disorder of glycosylation Id congenital disorder of glycosylation
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
207958	ALG11 alpha-1,2-mannosyltransferase	Alg11	Mus musculus (house mouse)	congenital disorder of glycosylation Ip
207839	polypeptide N-acetylgalactosaminyltransferase 6	Galnt6	Mus musculus (house mouse)
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
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
201562	3-hydroxyacyl-CoA dehydratase 2	HACD2 Aliases: Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	Homo sapiens (human)	cancer
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
200186	CREB regulated transcription coactivator 2	CRTC2	Homo sapiens (human)	type 2 diabetes mellitus
200185	keratinocyte associated protein 2	KRTCAP2 Aliases: KCP2	Homo sapiens (human)
199857	ALG14 UDP-N-acetylglucosaminyltransferase subunit	ALG14 Aliases: MGC19780	Homo sapiens (human)	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94
197322	acyl-CoA synthetase family member 3	ACSF3 Aliases: malonyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
197258	fucose kinase	FCSK Aliases: FLJ39408 L-fucose kinase	Homo sapiens (human)	congenital disorder of glycosylation congenital nystagmus dissociated nystagmus epilepsy esophagitis gastroesophageal reflux disease hypertropia intellectual disability learning disability mechanical strabismus ophthalmoplegia optic atrophy pathologic nystagmus peptic esophagitis spontaneous ocular nystagmus strabismus visual epilepsy
197257	lactate dehydrogenase D	LDHD	Homo sapiens (human)	aniridia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma intellectual disability learning disability microcephaly nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
197021	lactase like	LCTL Aliases: FLJ33279 KL lactase phlorizin hydrolase KLG KLPH gammaklotho klotho gamma	Homo sapiens (human)	arthritis arthropathy kidney disease osteoarthritis
196051	phospholipid phosphatase 4	PLPP4 Aliases: DPPL2 diacylglycerol pyrophosphate phosphatase-like 2	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 Pick's disease Reye syndrome breast cancer bronchus cancer bronchus carcinoma cerebral degeneration lung cancer lung carcinoma lung squamous cell carcinoma prostate cancer prostate carcinoma
195646	heparan sulfate (glucosamine) 3-O-sulfotransferase 2	Hs3st2	Mus musculus (house mouse)	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
192361	protein phosphatase 1, regulatory (inhibitor) subunit 2	Ppp1r2	Rattus norvegicus (Norway rat)
192334	beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)	b3gat3	Danio rerio (zebrafish)	Larsen-like syndrome B3GAT3 type
192315	UDP-glucuronate decarboxylase 1	uxs1	Danio rerio (zebrafish)

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