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 Name
- FOXL2 gene
- 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
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| fr-FR | French (France) | FOXL2 gène |
| 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; |
| pl-PL | Polish (Poland) | FOXL2 gen Synonyms: Gen FOXL2 |
| el-GR | Greek (Greece) | Γονίδιο FOXL2 Synonyms: Γονίδιο FOXL2 |
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://