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 |
---|---|---|
protein-containing complex | ||
plasma membrane | ||
Golgi cisterna membrane | ||
filopodium | ||
Golgi trans cisterna |
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 |
G06239NA
|
N-linked > O-linked |
G58896AZ
|
N-linked > O-linked | |
UDP-Gal |
G70874WW
|
N-linked > O-linked |
G84034JH
|
N-linked > O-linked | |
UDP-Gal |
G49108TO
|
G00055MO
|
|||
UDP-Gal |
G47557KS
|
O-glycan Synthesis |
G68007WG
|
O-glycan Synthesis | |
UDP-Gal |
G00033MO
|
O-glycan Synthesis |
G64973KT
|
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:0000007 | Autosomal recessive inheritance |
HP:0000219 | Thin upper lip vermilion |
HP:0000238 | Hydrocephalus |
HP:0000256 | Macrocephaly |
HP:0000316 | Hypertelorism |
HP:0000343 | Long philtrum |
HP:0000369 | Low-set ears |
HP:0000431 | Wide nasal bridge |
HP:0000545 | Myopia |
HP:0000821 | Hypothyroidism |
Disease ID | Disease Name |
---|---|
OMIM:607091 |
|
ORPHA:79332 |
|
OMIM:620364 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
100010600 | MONDO28244 | |||
100068209 | HORSE22196 | |||
100075703 | ORNAN32498 | |||
100145518 | Xenbase:XB-GENE-5871724 | |||
100223650 | TAEGU31271 | |||
100385157 | CALJA18761 | |||
100438031 | 9601_0:0028ed | PONAB36354 | ||
100477164 | AILME05607 | |||
100511655 | PIGXX00469 | |||
100613700 | 9598_0:002a43 | PANTR43800 |
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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