UniProt | Protein Name |
---|---|
P15291 |
|
GO Term | Evidence Code | PMID |
---|---|---|
angiogenesis involved in wound healing | ||
epithelial cell development | ||
binding of sperm to zona pellucida | ||
macrophage migration | ||
oligosaccharide biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
UDP-galactosyltransferase activity | ||
lactose synthase activity | ||
beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase activity | ||
manganese ion binding | ||
identical protein binding |
Gene Ontology |
---|
galactosyltransferase activity |
glycosylation |
transferase activity |
InterPro |
---|
Beta-1,4-galactosyltransferase |
Galactosyltransferase, C-terminal |
Galactosyltransferase, N-terminal |
Nucleotide-diphospho-sugar transferases |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Donor | Acceptor | Reducing terminal(Acceptor) | Product | Reducing terminal(Product) | Reference |
---|---|---|---|---|---|
UDP-Gal |
G32426JY
|
O-glycan Synthesis |
G94514IB
|
O-glycan Synthesis | |
UDP-Gal |
G23000DQ
|
octyl |
G80671XL
|
octyl | |
UDP-Gal |
G94541HG
|
O-glycan Synthesis |
G32877EI
|
O-glycan Synthesis | |
UDP-Gal |
G23438NR
|
O-glycan Synthesis |
G07932PU
|
O-glycan Synthesis | |
UDP-Gal |
G85608AG
|
O-glycan Synthesis |
G46748BU
|
O-glycan Synthesis |
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | XP_342821 | XM_342821 |
Mus musculus | NP_071641 | NM_022305 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0070256 | congenital disorder of glycosylation type IId | |
DOID:28 | endocrine system disease | |
DOID:2986 | IgA glomerulonephritis | |
DOID:5212 | congenital disorder of glycosylation |
HPO ID | HPO Term |
---|---|
HP:0003563 | Decreased LDL cholesterol concentration |
HP:0003577 | Congenital onset |
HP:0003645 | Prolonged partial thromboplastin time |
HP:0004855 | Reduced protein S activity |
HP:0005543 | Reduced protein C activity |
HP:0005989 | Redundant neck skin |
HP:0008947 | Infantile muscular hypotonia |
HP:0009062 | Infantile axial hypotonia |
HP:0011003 | High myopia |
HP:0011123 | Inflammatory abnormality of the skin |
Disease ID | Disease Name |
---|---|
OMIM:607091 |
|
ORPHA:79332 |
|
OMIM:620364 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
113583542 | ELEEL32107 | |||
113587936 | ELEEL40055 | |||
113897347 | BOBOX31047 | |||
114587454 | PODMU24397 | |||
115049667 | ECHNA28580 | |||
115050211 | ECHNA28887 | |||
115171563 | SALTR44144 | |||
115191838 | SALTR31444 | |||
115191839 | SALTR31447 | |||
115202190 | SALTR16714 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024