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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 **1526 - 1550** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
346606	monoacylglycerol O-acyltransferase 3	MOGAT3 Aliases: DC7 DGAT2L2 MGAT3	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 cerebral degeneration steatotic liver disease
346689	killer cell lectin like receptor G2	KLRG2 Aliases: C-type lectin domain family 15, member B CLEC15B FLJ44186	Homo sapiens (human)	prostate cancer prostate carcinoma
347404	LanC like family member 3	LANCL3	Homo sapiens (human)
347527	arylsulfatase family member H	ARSH	Homo sapiens (human)	Marfan syndrome Richter's syndrome X-linked chondrodysplasia punctata 1 acquired immunodeficiency syndrome acrodermatitis alcoholic liver cirrhosis autosomal dominant chondrodysplasia punctata cancer childhood leukemia chondrodysplasia punctata chronic lymphocytic leukemia dermatitis dyschromatosis symmetrica hereditaria essential thrombocythemia gallbladder disease hepatitis human immunodeficiency virus infectious disease leukemia liver cirrhosis liver disease microphthalmia mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis myelodysplastic syndrome neuroblastoma obsolete Matthew-Wood syndrome oculocerebrorenal syndrome rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 situs inversus tuberous sclerosis ventricular septal defect
347734	solute carrier family 35 member B2	SLC35B2 Aliases: UGTrel4	Homo sapiens (human)	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, mixed cellularity Langerhans cell sarcoma Langerhans-cell histiocytosis Richter's syndrome adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood lymphoma chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia dendritic cell sarcoma dilated cardiomyopathy 1A dilated cardiomyopathy follicular dendritic cell sarcoma follicular lymphoma hereditary multiple exostoses hypomyelinating leukodystrophy 26 interdigitating dendritic cell sarcoma invasive ductal carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma non-Hodgkin lymphoma obesity obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma reticulosarcoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood
348158	acyl-CoA synthetase medium chain family member 2B	ACSM2B Aliases: HXMA HYST1046 xenobiotic/medium chain fatty acid:CoA ligase	Homo sapiens (human)
348174	C-type lectin domain family 18 member A	CLEC18A	Homo sapiens (human)
349633	placenta expressed transcript 1	PLET1 Aliases: placenta-expressed transcript 1	Homo sapiens (human)	cancer embryoma
349667	reticulon 4 receptor like 2	RTN4RL2 Aliases: NGRH1 NgR2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
353091	retinoic acid early transcript 1G	RAET1G Aliases: ULBP5	Homo sapiens (human)	cancer
360203	glycosyltransferase 6 domain containing 1	GLT6D1	Homo sapiens (human)	acute pericementitis aggressive periodontitis periodontitis periodontosis
360226	serine protease 41	PRSS41	Homo sapiens (human)	ovarian cancer ovarian carcinoma
374378	polypeptide N-acetylgalactosaminyltransferase 18	GALNT18 Aliases: GALNT15 GalNAc-T18 MGC71806 polypeptide GalNAc transferase 18	Homo sapiens (human)	gastric adenocarcinoma rheumatoid arthritis
374907	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8	B3GNT8 Aliases: BGALT15 beta3Gn-T8	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
375775	patatin like phospholipase domain containing 7	PNPLA7 Aliases: FLJ31318 FLJ43070 FLJ44279 NTE-R1 NTEL1 RP11-48C7.2	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 blindness cerebellar ataxia cerebral degeneration hereditary spastic paraplegia neurodegenerative disease
375790	agrin	AGRN	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 Bell's palsy Pick's disease Reye syndrome acute myeloid leukemia agnosia cancer central sleep apnea cerebral degeneration congenital myasthenic syndrome 10 congenital myasthenic syndrome 8 congenital myasthenic syndrome congenital nystagmus congenital ptosis critical illness polyneuropathy developmental coordination disorder dissociated nystagmus embryoma epilepsy esophagitis esotropia facial nerve disease facial paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gastroesophageal reflux disease intellectual disability learning disability lung adenocarcinoma lung cancer monocular esotropia obstructive sleep apnea ophthalmoplegia papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peptic esophagitis polyhydramnios polyneuropathy progressive bulbar palsy ptosis scoliosis sensorineural hearing loss spontaneous ocular nystagmus thyroid gland papillary carcinoma visual epilepsy
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Homo sapiens (human)	Lafora disease
387712	enolase 4	ENO4 Aliases: AC023283.3	Homo sapiens (human)	male infertility
387837	C-type lectin domain family 12 member B	CLEC12B	Homo sapiens (human)	cancer cholesteatoma embryoma polyp of middle ear
388512	C-type lectin domain containing 17A	CLEC17A Aliases: FLJ45910 prolectin	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia
388581	C1q and TNF related 12	C1QTNF12	Homo sapiens (human)
389852	sperm acrosome associated 5	SPACA5 Aliases: LYC5 LYZL5 PNPK6288 SLLP2 Sperm Lysozyme-Like Protein 2 UNQ6288 dJ54B20.3	Homo sapiens (human)
390243	IZUMO1 receptor, JUNO	IZUMO1R Aliases: Folbp3 JUNO	Homo sapiens (human)	cancer
390637	GDP-D-glucose phosphorylase 1	GDPGP1	Homo sapiens (human)
391013	phospholipase A2 group IIC	PLA2G2C	Homo sapiens (human)

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