ret proto-oncogene
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Introduction
10q11.2
Expression
at least four different transcripts
Pathology
- loss of function mutations in the ret gene induces Hirschsprung's disease
- in contrast, activating mutations in the ret gene are associated with multiple endocrine neoplasia types 2A & 2B & familial medullary thyroid carcinoma, & 20-30% of papillary thyroid carcinomas
More general terms
Additional terms
- familial medullary thyroid carcinoma
- Hirschsprung disease; congenital megacolon; colonic aganglionosis; aganglionic megacolon
- multiple endocrine neoplasia type-2 (MEN-2)
- papillary thyroid carcinoma
References
- ↑ Hunter T. Cooperation between oncogenes. Cell. 1991 Jan 25;64(2):249-70. Review. PMID: https://www.ncbi.nlm.nih.gov/pubmed/1988147
- ↑ van Heyningen V. Genetics. One gene--four syndromes. Nature. 1994 Jan 27;367(6461):319-20. PMID: https://www.ncbi.nlm.nih.gov/pubmed/7906865