NOTCH4 Chromosome 6

Notch receptor 4
1 variant 1 Health Risk

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What This Gene Does
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 may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]
Gene Info
Gene Group
Notch receptors
Locus Type
gene with protein product
Location
6p21.32
Ensembl
ENSG00000204301
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS746443332 Health Risk Conflicting classifications of pathogenicity
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