LP269797-9
RET gene rearrangements
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Description
The RET gene (ret proto-oncogene) [HGNC Gene ID:9967] is located on chromosome 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 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, Jul 2008] [NCBI Gene ID:5979] Source: National Center for Biotechnology Information (NCBI) Gene
Basic Part Properties
- Part Display Name
- RET gene rearrangements
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2018-10-26
- Construct for LOINC Short Name
- RET gene rearrange
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- CodeSystem lookup
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Language Variants Get Info
Tag | Language | Translation |
---|---|---|
zh-CN | Chinese (China) | RET 基因重排 Synonyms: RET 基因重排(重组); |
es-ES | Spanish (Spain) | Reordenamiento del gen RET |
it-IT | Italian (Italy) | Riorganizzazioni del gene RET |
nl-NL | Dutch (Netherlands) | RET-genherschikking Synonyms: RET-gentranslocatie |
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