Nine novel germline gene variants in the RET proto-oncogene indentified in twelve unrelated cases

Syed A. Ahmed, Karen Snow-Bailey, W. Edward Highsmith, Weimin Sun, Raymond G. Fenwick, Rong Mao

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

We report nine novel DNA alterations in the RET proto-oncogene in 12 unrelated cases identified by DNA sequencing of exons 10 and 11 of the gene. The novel variants K666E, IVS9-11G→A, D631V in cis with H665Q, D631E (with C634Y), E623K (in trans with C618S), 616delGAG (in trans with C609Y), Y606C, C630R, and R635-T636insELCR;T636P were detected in patients with various clinical presentations ranging from thyroid goiter, medullary thyroid carcinoma, and pheochromocytoma to classic multiple endocrine neoplasia type 2A. When novel DNA alterations are found, extended family studies can be helpful in determining the clinical significance of such findings. Segregation within families suggests that K666E and T636insELCR;T636P are likely to be disease-causing mutations. However, the mechanism by which they affect the normal activity of the RET receptor is unclear. Absence of segregation with disease was observed for E623K and 616delGAG. For the remainder of the DNA alterations, family studies were not possible, and the clinical significance of these novel variants needs further assessment. Additional case reports, animal models, and/or functional studies are needed to determine the clinical significance of these newly identified variants.

Original languageEnglish (US)
Pages (from-to)283-288
Number of pages6
JournalJournal of Molecular Diagnostics
Volume7
Issue number2
DOIs
StatePublished - May 2005

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Medicine

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