AalsesAIAsk AI about NOTCH1
Gene Library · alsesAI

NOTCH1 gene

notch receptor 1

Key facts

Official symbol
NOTCH1
Full name
NOTCH1
Chromosome
9
Map location
9q34.3
Organism
Homo sapiens
NCBI Gene ID
4851
Also known as
AOS5, AOVD1, TAN1, hN1

Function summary

This gene encodes a member of the NOTCH family of proteins. Members of this Type I 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 signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016].

Go deeper with alsesAI

Ask anything about NOTCH1 — pathways, variants, literature, experimental design. Free for researchers, 30,000 AI tokens daily.

Ask AI about NOTCH1 →

Explore more genes

Data source: NCBI Gene · alsesAI Gene Library