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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 **415026 - 415050** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
23426	glutamate receptor interacting protein 1	GRIP1	Homo sapiens (human)
23424	tudor domain containing 7	TDRD7	Homo sapiens (human)
23423	transmembrane p24 trafficking protein 3	TMED3 Aliases: p24B p24g4 p24gamma4	Homo sapiens (human)	Nijmegen breakage syndrome anemia bacterial sepsis breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy fundus albipunctatus hepatocellular carcinoma large intestine cancer liver cancer macrocytic anemia nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma
23420	NODAL modulator 1	NOMO1	Homo sapiens (human)
23418	crumbs cell polarity complex component 1	CRB1	Homo sapiens (human)
23417	malonyl-CoA decarboxylase	MLYCD Aliases: MCD hMCD	Homo sapiens (human)	Castleman disease Kaposi's sarcoma Kimura disease Laron syndrome Marfan syndrome Meesmann corneal dystrophy Schmid metaphyseal chondrodysplasia Senior-Loken syndrome achondroplasia acquired immunodeficiency syndrome acute kidney tubular necrosis adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cancer cardiomyopathy central nervous system lymphoma childhood lymphoma choline deficiency disease diabetes mellitus diarrhea endomyocardial fibrosis epilepsy essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hypoglycemia inherited metabolic disorder kidney disease lactic acidosis lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macular corneal dystrophy membranous glomerulonephritis metabolic dysfunction-associated steatotic liver disease microphthalmia multicentric Castleman disease nasopharynx carcinoma nephritis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome normal pressure hydrocephalus obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete ymphosarcoma oral tuberculosis primary immunodeficiency disease pyoureter situs inversus steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood tuberculosis tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus visual epilepsy
23416	potassium voltage-gated channel subfamily H member 3	KCNH3	Homo sapiens (human)
23415	potassium voltage-gated channel subfamily H member 4	KCNH4	Homo sapiens (human)
23411	sirtuin 1	SIRT1	Homo sapiens (human)
23410	sirtuin 3	SIRT3	Homo sapiens (human)
23409	sirtuin 4	SIRT4 Aliases: SIR2L4	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma HELLP syndrome Zollinger-Ellison syndrome acute myocardial infarction adenocarcinoma adenoma arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy centronuclear myopathy colorectal cancer colorectal carcinoma congenital structural myopathy coronary artery disease coronary thrombosis cribriform carcinoma cytochrome-c oxidase deficiency disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis esophagus squamous cell carcinoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma hyperinsulinism hypertrophic cardiomyopathy large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease myocardial infarction neuroblastoma nutmeg liver obesity obsolete ymphosarcoma pancreatic cancer pancreatic carcinoma pre-eclampsia retinal disease retinitis silent myocardial infarction squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma transient myeloproliferative syndrome tubular adenocarcinoma tubular aggregate myopathy 1 type 2 diabetes mellitus uterine corpus cancer
23408	sirtuin 5	SIRT5	Homo sapiens (human)
23405	dicer 1, ribonuclease III	DICER1	Homo sapiens (human)
23404	exosome component 2	EXOSC2	Homo sapiens (human)
23400	ATPase cation transporting 13A2	ATP13A2	Homo sapiens (human)
23398	peptidylprolyl isomerase domain and WD repeat containing 1	PPWD1	Homo sapiens (human)
23396	phosphatidylinositol-4-phosphate 5-kinase type 1 gamma	PIP5K1C Aliases: KIAA0589 LCCS3 PIP5Kgamma	Homo sapiens (human)	breast cancer breast carcinoma cancer invasive ductal carcinoma lethal congenital contracture syndrome 3 rabies
23395	leucyl-tRNA synthetase 2, mitochondrial	LARS2	Homo sapiens (human)
23394	activity dependent neuroprotector homeobox	ADNP	Homo sapiens (human)
23392	Ecm29 proteasome adaptor and scaffold	ECPAS	Homo sapiens (human)
23389	mediator complex subunit 13L	MED13L	Homo sapiens (human)
23387	SIK family kinase 3	SIK3	Homo sapiens (human)
23385	nicastrin	NCSTN	Homo sapiens (human)
23384	sperm antigen with calponin homology and coiled-coil domains 1 like	SPECC1L	Homo sapiens (human)
23383	MAU2 sister chromatid cohesion factor	MAU2	Homo sapiens (human)

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