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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 **26 - 50** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
493869	glutathione peroxidase 8 (putative)	GPX8 Aliases: EPLA847 UNQ847	Homo sapiens (human)
442117	polypeptide N-acetylgalactosaminyltransferase like 6	GALNTL6 Aliases: GALNT17 GalNAc-T6L polypeptide GalNAc transferase-like 6	Homo sapiens (human)	nicotine dependence
441531	phosphoglycerate mutase family member 4	PGAM4 Aliases: PGAM-B PGAM1 PGAM3 dJ1000K24.1	Homo sapiens (human)	male infertility
440138	ALG11 alpha-1,2-mannosyltransferase	ALG11 Aliases: CDG1P GDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase KIAA0266	Homo sapiens (human)	cerebral degeneration congenital disorder of glycosylation Ip congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia inherited metabolic disorder intellectual disability learning disability mechanical strabismus microcephaly ophthalmoplegia scoliosis sensorineural hearing loss strabismus visual epilepsy
414328	IDNK gluconokinase	IDNK Aliases: bA522I20.2 hGntK	Homo sapiens (human)
402635	galectin-related inter-fiber protein	GRIFIN	Homo sapiens (human)
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Aliases: Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer
391013	phospholipase A2 group IIC	PLA2G2C	Homo sapiens (human)
390637	GDP-D-glucose phosphorylase 1	GDPGP1	Homo sapiens (human)
390243	IZUMO1 receptor, JUNO	IZUMO1R Aliases: Folbp3 JUNO	Homo sapiens (human)	cancer
389852	sperm acrosome associated 5	SPACA5 Aliases: LYC5 LYZL5 PNPK6288 SLLP2 Sperm Lysozyme-Like Protein 2 UNQ6288 dJ54B20.3	Homo sapiens (human)
388581	C1q and TNF related 12	C1QTNF12	Homo sapiens (human)
388512	C-type lectin domain containing 17A	CLEC17A Aliases: FLJ45910 prolectin	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia
387837	C-type lectin domain family 12 member B	CLEC12B	Homo sapiens (human)	cancer cholesteatoma embryoma polyp of middle ear
387712	enolase 4	ENO4 Aliases: AC023283.3	Homo sapiens (human)	male infertility
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Homo sapiens (human)	Lafora 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
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
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
374378	polypeptide N-acetylgalactosaminyltransferase 18	GALNT18 Aliases: GALNT15 GalNAc-T18 MGC71806 polypeptide GalNAc transferase 18	Homo sapiens (human)	gastric adenocarcinoma rheumatoid arthritis
360226	serine protease 41	PRSS41	Homo sapiens (human)	ovarian cancer ovarian carcinoma
360203	glycosyltransferase 6 domain containing 1	GLT6D1	Homo sapiens (human)	acute pericementitis aggressive periodontitis periodontitis periodontosis
353091	retinoic acid early transcript 1G	RAET1G Aliases: ULBP5	Homo sapiens (human)	cancer
349667	reticulon 4 receptor like 2	RTN4RL2 Aliases: NGRH1 NgR2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
349633	placenta expressed transcript 1	PLET1 Aliases: placenta-expressed transcript 1	Homo sapiens (human)	cancer embryoma

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