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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 **420976 - 421000** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
3630	insulin	INS	Homo sapiens (human)	Alzheimer's disease cholangiocarcinoma diabetes mellitus diabetic retinopathy disease of metabolism gestational diabetes hyperinsulinism hypertension hyperuricemia insulinoma maturity-onset diabetes of the young type 10 maturity-onset diabetes of the young neonatal diabetes osteoarthritis pancreatic cancer pancreatic ductal carcinoma permanent neonatal diabetes mellitus prostate cancer steatotic liver disease type 1 diabetes mellitus 2 type 1 diabetes mellitus type 2 diabetes mellitus
3628	inositol polyphosphate-1-phosphatase	INPP1	Homo sapiens (human)	bipolar disorder cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer obsolete major affective disorder 2
3626	inhibin subunit beta C	INHBC	Homo sapiens (human)
3625	inhibin subunit beta B	INHBB	Homo sapiens (human)
3624	inhibin subunit beta A	INHBA	Homo sapiens (human)
3623	inhibin subunit alpha	INHA	Homo sapiens (human)
3619	inner centromere protein	INCENP	Homo sapiens (human)
3617	interphotoreceptor matrix proteoglycan 1	IMPG1	Homo sapiens (human)
3615	inosine monophosphate dehydrogenase 2	IMPDH2	Homo sapiens (human)
3613	inositol monophosphatase 2	IMPA2 Aliases: myo-inositol monophosphatase 2	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis intermittent explosive disorder major depressive disorder melancholic depression mood disorder neurotic disorder nonpapillary renal cell carcinoma obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
3612	inositol monophosphatase 1	IMPA1 Aliases: myo-inositol monophosphatase 1	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 Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive intellectual developmental disorder 59 autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
3609	interleukin enhancer binding factor 3	ILF3	Homo sapiens (human)
3608	interleukin enhancer binding factor 2	ILF2	Homo sapiens (human)
3607	forkhead box K2	FOXK2	Homo sapiens (human)
3605	interleukin 17A	IL17A	Homo sapiens (human)
3604	TNF receptor superfamily member 9	TNFRSF9	Homo sapiens (human)
3603	interleukin 16	IL16	Homo sapiens (human)
3601	interleukin 15 receptor subunit alpha	IL15RA	Homo sapiens (human)
3600	interleukin 15	IL15	Homo sapiens (human)
3598	interleukin 13 receptor subunit alpha 2	IL13RA2	Homo sapiens (human)
3597	interleukin 13 receptor subunit alpha 1	IL13RA1	Homo sapiens (human)
3596	interleukin 13	IL13	Homo sapiens (human)
3595	interleukin 12 receptor subunit beta 2	IL12RB2	Homo sapiens (human)
3594	interleukin 12 receptor subunit beta 1	IL12RB1	Homo sapiens (human)
3593	interleukin 12B	IL12B	Homo sapiens (human)

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