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RET gene

ret proto-oncogene

Key facts

Official symbol
RET
Full name
RET
Chromosome
10
Map location
10q11.21
Organism
Homo sapiens
NCBI Gene ID
5979
Also known as
CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1

Function summary

This gene encodes a transmembrane receptor and member of the tyrosine protein kinase family of proteins. Binding of ligands such as GDNF (glial cell-line derived neurotrophic factor) and other related proteins to the encoded receptor stimulates receptor dimerization and activation of downstream signaling pathways that play a role in cell differentiation, growth, migration and survival. The encoded receptor is important in development of the nervous system, and the development of organs and tissues derived from the neural crest. This proto-oncogene can undergo oncogenic activation through both cytogenetic rearrangement and activating point mutations. Mutations in this gene are associated with Hirschsprung disease and central hypoventilation syndrome and have been identified in patients with renal agenesis. [provided by RefSeq, Sep 2017].

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Data source: NCBI Gene · alsesAI Gene Library