Statements (15)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
congenital disorder of glycosylation type I
|
| gptkbp:encodes |
ST3 beta-galactoside alpha-2,3-sialyltransferase 3
|
| gptkbp:Entrez_Gene_ID |
ENSG00000115935
11052 |
| gptkbp:expressedIn |
various human tissues
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
catalyzes N-linked glycosylation
|
| gptkbp:HGNC_ID |
HGNC:11457
|
| https://www.w3.org/2000/01/rdf-schema#label |
STT3B
|
| gptkbp:locatedOnChromosome |
chromosome 2
|
| gptkbp:orthologIn |
gptkb:Mus_musculus
|
| gptkbp:UniProtID |
Q8TCJ2
|
| gptkbp:bfsParent |
gptkb:oligosaccharyltransferase_complex
|
| gptkbp:bfsLayer |
8
|