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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 .

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 "galactosyltransferase activity"

Displaying entries **51 - 75** of **11012** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
51148	cerebral endothelial cell adhesion molecule	CERCAM	Homo sapiens (human)
53418	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	B4galt2	Mus musculus (house mouse)
53947	alpha 1,4-galactosyltransferase (P1PK blood group)	A4GALT Aliases: A14GALT CD77 synthase Gb3 synthase Gb3S P(k) globotriaosylceramide synthase lactosylceramide 4-alpha-galactosyltransferase	Homo sapiens (human)	Burkitt lymphoma Caffey disease acute megakaryocytic leukemia adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma granular cell carcinoma hematologic cancer hemolytic-uremic syndrome kidney failure leukemia teratocarcinoma thrombophilia tubular adenocarcinoma
54218	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 4	B3galt4	Mus musculus (house mouse)
56336	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	B4galt5	Mus musculus (house mouse)	multiple sclerosis
56375	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 4	B4galt4	Mus musculus (house mouse)
56386	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 6	B4galt6	Mus musculus (house mouse)	multiple sclerosis
56913	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C1GALT1 Aliases: C1GALT T-synthase core 1 beta3-Gal-T	Homo sapiens (human)	Henoch-Schoenlein purpura IgA glomerulonephritis Tn polyagglutination syndrome adenocarcinoma adenoma autoimmune disease of blood autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hypersensitivity vasculitis immune system disease kidney disease large intestine cancer liver cancer microphthalmia nephritis nephrosis obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma pyoureter sarcomatoid carcinoma thrombocytopenia tubular adenocarcinoma type 2 diabetes mellitus
57370	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	B4galt3	Mus musculus (house mouse)
59048	C1GALT1-specific chaperone 1	C1galt1c1	Mus musculus (house mouse)	Tn polyagglutination syndrome hemolytic-uremic syndrome
63888	alpha 1,4-galactosyltransferase	A4galt	Rattus norvegicus (Norway rat)
65044	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	Rattus norvegicus (Norway rat)	autoimmune disease of blood
65196	beta-1,4-galactosyltransferase 6	B4galt6	Rattus norvegicus (Norway rat)	multiple sclerosis
65270	histo-blood group ABO system transferase 3	Abo3	Rattus norvegicus (Norway rat)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
72145	WD repeat and FYVE domain containing 3	Wdfy3	Mus musculus (house mouse)	Chediak-Higashi syndrome autism spectrum disorder primary autosomal dominant microcephaly 18
75859	RIKEN cDNA 4930568D16 gene	4930568D16Rik	Mus musculus (house mouse)
79369	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4	B3GNT4 Aliases: B3GN-T4 beta3Gn-T4	Homo sapiens (human)
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
80908	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	Abo	Mus musculus (house mouse)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
84002	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5	B3GNT5 Aliases: B3GN-T5 beta3Gn-T5 lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase	Homo sapiens (human)	breast cancer breast carcinoma giant cell glioblastoma glioblastoma
93010	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3GNT7 Aliases: beta3GnT7	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
93961	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5	B3galt5	Mus musculus (house mouse)	pancreatic cancer
94192	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	Mus musculus (house mouse)	autoimmune disease of blood
117592	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	B3galt6	Mus musculus (house mouse)	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
126792	beta-1,3-galactosyltransferase 6	B3GALT6 Aliases: beta-1,3-galactosyltransferase-6 beta3GalT6	Homo sapiens (human)	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease spondyloepimetaphyseal dysplasia with joint laxity type 1 tendinitis ventricular septal defect

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