LP420119-2
FOXL2 gene
Active
Description
The FOXL2 (forkhead box L2) gene [HGNC Gene ID: 1092] is located on chromosome 3 at position q22.3. This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016][NCBI Gene ID: 668] Source: National Center for Biotechnology Information (NCBI) Gene
Basic Part Properties
- Part Display Name
- FOXL2 gene
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2020-08-18
- Construct for LOINC Short Name
- FOXL2
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LP420119-2 - ConceptMap translate
- https:
//fhir.loinc.org/ConceptMap/$translate?system=http: //loinc.org&code=LP420119-2
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| it-IT | Italian (Italy) | FOXL2, gene |
| nl-NL | Dutch (Netherlands) | FOXL2-gen |
| es-ES | Spanish (Spain) | Gen FOXL2 |
| zh-CN | Chinese (China) | FOXL2 基因 Synonyms: Forkhead Box L2 基因; |
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