UniProt | Protein Name |
---|---|
P15291 |
|
GO Term | Evidence Code | PMID |
---|---|---|
extracellular matrix organization | ||
positive regulation of apoptotic process | ||
positive regulation of epithelial cell proliferation involved in wound healing | ||
negative regulation of epithelial cell proliferation | ||
lipid metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
beta-tubulin binding | ||
N-acetyllactosamine synthase activity | ||
cytoskeletal protein binding |
|
|
alpha-tubulin binding | ||
galactosyltransferase activity |
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 |
---|---|---|---|---|
100620048 | SHEEP08882 | |||
100659897 | LOXAF17408 | |||
100692426 | ORENI47747 | |||
100692970 | ORENI47747 | |||
100860927 | CAPHI29365 | |||
100962109 | OTOGA03226 | |||
100974756 | 9597_0:002852 | PANPA39378 | ||
101022281 | PAPAN07978 | |||
101054125 | SAIBB32165 | |||
101066088 | TAKRU00474 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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