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NOTCH2

NOTCH2
Protein NOTCH2 PDB 2oo4.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases NOTCH2, AGS2, HJCYS, hN2, Notch-2, notch 2
External IDs MGI: 97364 HomoloGene: 7865 GeneCards: NOTCH2
RNA expression pattern
PBB GE NOTCH2 202443 x at tn.png

PBB GE NOTCH2 202445 s at tn.png

PBB GE NOTCH2 212377 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001200001
NM_024408

NM_010928

RefSeq (protein)

NP_001186930
NP_077719

NP_035058.2
NP_035058

Location (UCSC) Chr 1: 119.91 – 120.07 Mb Chr 3: 98.01 – 98.15 Mb
PubMed search

2OO4

NM_001200001
NM_024408

NM_010928

NP_001186930
NP_077719

NP_035058.2
NP_035058

Neurogenic locus notch homolog protein 2 also known as notch 2 is a protein that in humans is encoded by the NOTCH2 gene.

NOTCH2 is associated with Alagille syndrome and Hajdu–Cheney syndrome.

Notch 2 is a member of the notch family. Members of this Type 1 transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple, different domain types. Notch family members play a role in a variety of developmental processes by controlling cell fate decisions. The Notch signaling network is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signaling pathway that plays a key role in development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remain to be determined. This protein is cleaved in the trans-Golgi network, and presented on the cell surface as a heterodimer. This protein functions as a receptor for membrane bound ligands, and may play a role in vascular, renal and hepatic development.


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