Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:Alagille_syndrome
gptkb:Hajdu-Cheney_syndrome |
| gptkbp:biologicalProcess |
gptkb:Notch_signaling_pathway
cell fate determination receptor activity |
| gptkbp:encodes |
gptkb:Neurogenic_locus_notch_homolog_protein_2
|
| gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000134250
4853 |
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:HGNC_ID |
7882
|
| https://www.w3.org/2000/01/rdf-schema#label |
human NOTCH2 gene
|
| gptkbp:locatedOnChromosome |
chromosome 1
1p12 |
| gptkbp:OMIM |
600275
|
| gptkbp:orthologInMouse |
gptkb:Notch2
|
| gptkbp:tissue_specificity |
gptkb:kidney
brain liver |
| gptkbp:UniProtID |
gptkb:Q04721
|
| gptkbp:bfsParent |
gptkb:Notch_gene
|
| gptkbp:bfsLayer |
6
|