RET

Aliases 
CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC, PTC, RET-ELE1, RET51
Chromosomal Locations 
10q11.2

This gene, a member of the cadherin superfamily, encodes one of the receptor tyrosine kinases, which are cell-surface molecules that transduce signals for cell growth and differentiation. This gene plays a crucial role in neural crest development, and it can undergo oncogneic activation in vivo and in vitro by cytogenetic rearrangement.

Mutations in this gene are associated with the disorders multiple endocrine neoplasia, type IIA, multiple endocrine neoplasia, type IIB, Hirschsprung disease, and medullary thryoid carcinoma. Two transcript variants encoding different isoforms have been found for this gene.

Additional transcript variants have been described but their bioological validity has not been confirmed.

Description 
ret proto-oncogene RET transforming sequence cadherin family member 12 cadherin-related family member 16 hydroxyaryl-protein kinase proto-oncogene c-Ret proto-oncogene tyrosine-protein kinase receptor Ret receptor tyrosine kinase ret proto-oncogene (multiple endocrine neoplasia and medullary thryoid carcinoma 1, Hirschsprung disease)