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NOTCH4

NOTCH4
Identifiers
Aliases NOTCH4, INT3, notch 4
External IDs MGI: 107471 HomoloGene: 3351 GeneCards: NOTCH4
Genetically Related Diseases
schizophrenia, age related macular degeneration, asthma, systemic scleroderma
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004557

NM_010929

RefSeq (protein)

NP_004548

NP_035059.2
NP_035059

Location (UCSC) Chr 6: 32.19 – 32.22 Mb Chr 17: 34.56 – 34.59 Mb
PubMed search

NM_004557

NM_010929

NP_004548

NP_035059.2
NP_035059

Neurogenic locus notch homolog 4 also known as notch 4 is a protein that in humans is encoded by the NOTCH4 gene located on chromosome 6.

An alternative splice variant of the NOTCH4 gene has been described, but its biological significance has not been determined.

The neurogenic locus notch homolog 4 protein is a member of the Notch family. Members of this type 1 transmembrane protein family share structural characteristics. These include an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain that consists of multiple, but different, domain types.

Notch protein family members play a role in a variety of developmental processes by controlling cell fate decisions. The Notch signaling pathway is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells


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