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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 **8976 - 9000** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
4436	mutS homolog 2	MSH2	Homo sapiens (human)
55898	unc-45 myosin chaperone A	UNC45A	Homo sapiens (human)
22989	myosin heavy chain 15	MYH15	Homo sapiens (human)
10499	nuclear receptor coactivator 2	NCOA2	Homo sapiens (human)
57169	zinc finger NFX1-type containing 1	ZNFX1	Homo sapiens (human)
6633	small nuclear ribonucleoprotein D2 polypeptide	SNRPD2	Homo sapiens (human)
57332	chromobox 8	CBX8	Homo sapiens (human)
5099	protocadherin 7	PCDH7	Homo sapiens (human)
131096	potassium voltage-gated channel subfamily H member 8	KCNH8	Homo sapiens (human)
23600	alpha-methylacyl-CoA racemase	AMACR Aliases: P504S RACE	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Ewing sarcoma Gilbert syndrome Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis MHC class II deficiency Marfan syndrome Rett syndrome acinar cell carcinoma acute myeloid leukemia adenocarcinoma adenoma adenosine deaminase deficiency agenesis of the corpus callosum with peripheral neuropathy alpha-methylacyl-CoA racemase deficiency atrial fibrillation atrophy of prostate bilirubin metabolic disorder bladder carcinoma blindness blood coagulation disease brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cholestasis chondroma chondrosarcoma chromophobe renal cell carcinoma chronic kidney disease clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cone-rod dystrophy congenital bile acid synthesis defect 4 congenital bile acid synthesis defect congestive heart failure cribriform carcinoma cutaneous fibrous histiocytoma dengue disease depressive disorder diabetes mellitus diffuse large B-cell lymphoma dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer epilepsy esophagus adenocarcinoma essential hypertension essential thrombocythemia follicular adenoma fundus albipunctatus gallbladder disease gastrointestinal stromal tumor germ cell and embryonal cancer germ cell cancer germinoma gliosarcoma granular cell carcinoma heart disease hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hidradenoma high grade glioma hypertension hypogonadism inflammatory bowel disease 1 inflammatory bowel disease inflammatory myofibroblastic tumor intrahepatic cholestasis kidney cancer kwashiorkor large intestine cancer lipoma liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder marasmus mastitis medulloblastoma medulloepithelioma melancholic depression melanoma microcystic adenoma migraine mixed glioma motor neuritis motor peripheral neuropathy multiple sclerosis multiple symmetric lipomatosis myelodysplastic syndrome nasopharynx carcinoma neuritis neuroblastoma neuroectodermal tumor neuroendocrine carcinoma neuropathy neurotic disorder nodular prostate nonpapillary renal cell carcinoma nutrition disease obesity obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obsolete ymphosarcoma oxyphilic adenoma pancreatic cancer pancreatitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma papilloma peripheral nervous system disease peroxisomal disease pleomorphic lipoma primary cutaneous amyloidosis prostate adenocarcinoma prostate cancer prostate carcinoma in situ prostate carcinoma prostatic adenoma protein-energy malnutrition renal carcinoma renal cell carcinoma renal oncocytoma retinitis pigmentosa rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia severe combined immunodeficiency situs inversus skin melanoma skin papilloma skin tag squamous cell carcinoma squamous cell papilloma status epilepticus supratentorial primitive neuroectodermal tumor syringoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tuberculosis tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease visual epilepsy yellow fever
7174	tripeptidyl peptidase 2	TPP2	Homo sapiens (human)
3001	granzyme A	GZMA	Homo sapiens (human)
8325	frizzled class receptor 8	FZD8	Homo sapiens (human)
90522	Yip1 interacting factor homolog B, membrane trafficking protein	YIF1B	Homo sapiens (human)
91272	biorientation of chromosomes in cell division 1	BOD1	Homo sapiens (human)
28232	solute carrier organic anion transporter family member 3A1	SLCO3A1	Homo sapiens (human)
64714	protein disulfide isomerase family A member 2	PDIA2	Homo sapiens (human)
5345	serpin family F member 2	SERPINF2	Homo sapiens (human)
389549	FEZ family zinc finger 1	FEZF1	Homo sapiens (human)
54206	ERBB receptor feedback inhibitor 1	ERRFI1	Homo sapiens (human)	endometrial cancer osteoarthritis
931	membrane spanning 4-domains A1	MS4A1	Homo sapiens (human)
2856	G protein-coupled receptor 33	GPR33	Homo sapiens (human)
112770	glycosylated lysosomal membrane protein	GLMP	Homo sapiens (human)
7520	X-ray repair cross complementing 5	XRCC5	Homo sapiens (human)
23303	kinesin family member 13B	KIF13B	Homo sapiens (human)

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