Background
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 oncogenic 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 thyroid carcinoma. Two transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described but their biological validity has not been confirmed. [provided by RefSeq].
Product Information
Source: HEK293
| Purity: >95% by SDS-PAGE analysis
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Purification Method: FPLC
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Gene/Protein Information
Gene Name: RET
| Gene Symbol: CDHF12, HSCR1, MEN2A, MEN2B, MTC1, PTC, RETELE1, RET51
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Gene Name Synonyms: CDHF12, HSCR1, MEN2A, MEN2B, MTC1, PTC, RETELE1, RET51
| NCBI Acc#: NM_020975
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Chromosomal Location: 10q11.2
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