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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

Search results for "glycoprotein metabolic process"

Displaying entries **176 - 200** of **17753** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
42991	beta-4-galactosyltransferase 7	beta4GalT7	Drosophila melanogaster (fruit fly)	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
44433	Heparan sulfate 2-O-sulfotransferase	Hs2st	Drosophila melanogaster (fruit fly)
50515	carbohydrate sulfotransferase 11	CHST11 Aliases: C4ST C4ST1 C4St-1 HSA269537 chondroitin 4-sulfotransferase 1	Homo sapiens (human)	Barrett's esophagus Costello syndrome Richter's syndrome arthritis arthropathy breast cancer breast carcinoma cancer chronic lymphocytic leukemia hepatocellular carcinoma leukoencephalopathy with vanishing white matter liver cancer osteoarthritis ovarian cancer ovarian carcinoma schizophrenia scoliosis
50762	F-box protein 6	Fbxo6	Mus musculus (house mouse)
50785	heparan sulfate 6-O-sulfotransferase 1	Hs6st1	Mus musculus (house mouse)	hypogonadotropic hypogonadism 15 with or without anosmia
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Mus musculus (house mouse)	Paganini-Miozzo syndrome
50787	heparan sulfate 6-O-sulfotransferase 3	Hs6st3	Mus musculus (house mouse)
50935	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	St6galnac6	Mus musculus (house mouse)
51046	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	ST8SIA3 Aliases: ST8Sia III	Homo sapiens (human)	acute myeloid leukemia basal ganglia disease cancer embryoma schizophrenia
51146	alpha-1,4-N-acetylglucosaminyltransferase	A4GNT Aliases: alpha4GnT	Homo sapiens (human)	adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma gastritis granular cell carcinoma pancreatic cancer pancreatic carcinoma peptic ulcer disease stomach cancer stomach carcinoma tubular adenocarcinoma
52120	heparan-alpha-glucosaminide N-acetyltransferase	Hgsnat	Mus musculus (house mouse)
53618	fucosyltransferase 8	Fut8	Mus musculus (house mouse)	pulmonary emphysema
54616	exostosin-like glycosyltransferase 3	Extl3	Mus musculus (house mouse)	hereditary multiple exostoses
54710	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	Hs3st3b1	Mus musculus (house mouse)
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
55741	ER degradation enhancing alpha-mannosidase like protein 2	EDEM2 Aliases: FLJ10783 bA4204.1	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 Pick's disease Reye syndrome cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid
55757	UDP-glucose glycoprotein glucosyltransferase 2	UGGT2 Aliases: FLJ10873 FLJ11485 HUGT2 MGC117360 MGC150689 MGC87276 UDP-glucose:glycoprotein glucosyltransferase 2	Homo sapiens (human)	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma myocardial infarction silent myocardial infarction type 2 diabetes mellitus
55768	N-glycanase 1	NGLY1 Aliases: FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	Homo sapiens (human)	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
55790	chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 Aliases: CSGalNAcT-1 ChGn FLJ11264 chondroitin beta1,4 N-acetylgalactosaminyltransferase glucuronylgalactosylproteoglycan 4-beta-N- acetylgalactosaminyltransferase	Homo sapiens (human)	Guillain-Barre syndrome Laron syndrome Miller Fisher syndrome achondroplasia anorexia nervosa breast cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetic ketoacidosis large intestine cancer melanoma multiple sclerosis obsolete type 1 diabetes mellitus 9 skin melanoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
55959	sulfatase 2	SULF2 Aliases: HSULF-2 KIAA1247 SULF-2	Homo sapiens (human)	acute pancreatitis adenocarcinoma adenoma arthritis arthropathy brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometriosis of ovary endometriosis of uterus endometriosis essential hypertension giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma hyperlipoproteinemia type III hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis invasive ductal carcinoma large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma parapsoriasis postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma psoriasis pulmonary fibrosis pure red-cell aplasia pustulosis of palm and sole renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma skin benign neoplasm skin cancer squamous cell carcinoma stomach cancer stomach carcinoma testicular cancer testis seminoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uveal melanoma
56219	exostosin-like glycosyltransferase 1	Extl1	Mus musculus (house mouse)	hereditary multiple exostoses
56336	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	B4galt5	Mus musculus (house mouse)	multiple sclerosis
56819	exostosin-like glycosyltransferase 3	Extl3	Rattus norvegicus (Norway rat)	hereditary multiple exostoses
56886	UDP-glucose glycoprotein glucosyltransferase 1	UGGT1 Aliases: HUGT1	Homo sapiens (human)	Crigler-Najjar syndrome Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha 1-antitrypsin deficiency beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis embryoma epilepsy gallbladder disease hepatitis C hepatitis D leukopenia liver disease neonatal jaundice neutropenia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia visual epilepsy xeroderma pigmentosum group D

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