Statements (29)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
gptkb:gene |
| gptkbp:alternativeSplicing |
yes
|
| gptkbp:associatedWith |
gptkb:Alagille_syndrome
gptkb:Hajdu-Cheney_syndrome |
| gptkbp:encodes |
gptkb:Neurogenic_locus_notch_homolog_protein_2
|
| gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000134250
4853 |
| gptkbp:expressedIn |
various tissues
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
cell fate determination
developmental processes |
| gptkbp:geneType |
protein-coding
|
| https://www.w3.org/2000/01/rdf-schema#label |
Notch2
|
| gptkbp:interactsWith |
gptkb:DLL1
gptkb:JAG1 gptkb:RBPJ |
| gptkbp:locatedOnChromosome |
chromosome 1p12
|
| gptkbp:memberOf |
gptkb:Notch_family
|
| gptkbp:mutationAssociatedWith |
congenital heart defects
skeletal abnormalities |
| gptkbp:OMIM |
600275
|
| gptkbp:orthologIn |
gptkb:Mus_musculus
gptkb:Drosophila_melanogaster |
| gptkbp:pathway |
gptkb:Notch_signaling_pathway
|
| gptkbp:product |
single-pass transmembrane receptor
|
| gptkbp:UniProtID |
gptkb:Q04721
|
| gptkbp:bfsParent |
gptkb:human_NOTCH2_gene
|
| gptkbp:bfsLayer |
7
|