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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 **7876 - 7900** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
970	CD70 molecule	CD70	Homo sapiens (human)
7001	peroxiredoxin 2	PRDX2	Homo sapiens (human)
26696	olfactory receptor family 2 subfamily T member 1	OR2T1	Homo sapiens (human)
8288	eosinophil peroxidase	EPX	Homo sapiens (human)
4062	lymphocyte antigen 6 family member H	LY6H	Homo sapiens (human)
9444	QKI, KH domain containing RNA binding	QKI	Homo sapiens (human)
997	cell division cycle 34, ubiqiutin conjugating enzyme	CDC34	Homo sapiens (human)
242	arachidonate 12-lipoxygenase, 12R type	ALOX12B Aliases: 12R-LOX 12R-lipoxygenase	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome achondroplasia acquired hyperkeratosis actinic keratosis adenocarcinoma adenoma 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 4B 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 bacterial sepsis bronchus cancer bronchus carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer cribriform carcinoma dermatitis ectropion epidermolytic hyperkeratosis granular cell carcinoma hypohidrosis hypotrichosis ichthyosis vulgaris ichthyosis intellectual disability keratitis keratoconjunctivitis keratosis follicularis kidney failure large intestine cancer learning disability lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mongolian spot nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma obsolete congenital ichthyosiform erythroderma otitis media ovarian cancer ovarian carcinoma palmoplantar keratosis pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis seminoma sensorineural hearing loss skin disease squamous cell carcinoma testicular cancer testicular germ cell cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma
4146	matrilin 1	MATN1	Homo sapiens (human)
3202	homeobox A5	HOXA5	Homo sapiens (human)
7936	negative elongation factor complex member E	NELFE	Homo sapiens (human)
51726	DnaJ heat shock protein family (Hsp40) member B11	DNAJB11	Homo sapiens (human)
1513	cathepsin K	CTSK	Homo sapiens (human)
3976	LIF interleukin 6 family cytokine	LIF	Homo sapiens (human)
54456	Mov10 like RNA helicase 1	MOV10L1	Homo sapiens (human)
1962	enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase	EHHADH	Homo sapiens (human)	D-bifunctional protein deficiency Fanconi renotubular syndrome 3 Fanconi syndrome Laron syndrome Zollinger-Ellison syndrome achondroplasia amyloidosis bipolar disorder cancer carnitine palmitoyltransferase II deficiency cystinosis cystinuria cytochrome-c oxidase deficiency disease familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hyperinsulinemic hypoglycemia hyperinsulinism liver cancer liver disease mitochondrial trifunctional protein deficiency osteomalacia prostate cancer prostate carcinoma proteinuria rickets spondyloepimetaphyseal dysplasia, Sponastrime type substance abuse substance-related disorder tuberculosis
10575	chaperonin containing TCP1 subunit 4	CCT4	Homo sapiens (human)
119587	carboxypeptidase X, M14 family member 2	CPXM2	Homo sapiens (human)
115207	potassium channel tetramerization domain containing 12	KCTD12	Homo sapiens (human)
27124	inositol polyphosphate-5-phosphatase J	INPP5J Aliases: INPP5 PIPP	Homo sapiens (human)	breast cancer breast carcinoma cancer
3419	isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha	IDH3A Aliases: H-IDH alpha NAD(H)-specific isocitrate dehydrogenase alpha subunit NAD+-specific ICDH isocitrate dehydrogenase (NAD+) alpha chain isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isocitric dehydrogenase	Homo sapiens (human)	Zollinger-Ellison syndrome alternating hemiplegia of childhood arthritis arthropathy autonomic neuropathy bipolar disorder blindness brain disease cancer cataract central nervous system disease cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus early infantile epileptic encephalopathy fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus learning disability lung adenocarcinoma lung cancer nervous system disease neuromuscular junction disease obesity obsolete asthenopia ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus primary open angle glaucoma retinitis pigmentosa 90 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
8642	dachsous cadherin-related 1	DCHS1	Homo sapiens (human)
121642	alkB homolog 2, alpha-ketoglutarate dependent dioxygenase	ALKBH2	Homo sapiens (human)
55504	TNF receptor superfamily member 19	TNFRSF19	Homo sapiens (human)
3707	inositol-trisphosphate 3-kinase B	ITPKB Aliases: IP3-3KB IP3KB	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 Pick's disease Reye syndrome allergic disease bronchus cancer bronchus carcinoma cancer cerebral degeneration dental caries dentin caries embryoma lung benign neoplasm lung cancer lung carcinoma obsolete ymphosarcoma sick sinus syndrome

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