Gene
FIGLA
folliculogenesis specific bHLH transcription factor
- HGNC 24669↗(opens in a new tab)
- Ensembl gene ENSG00000183733↗(opens in a new tab)
- NCBI Gene 344018↗(opens in a new tab)
Summary
- Cytogenetic location
- 2p13.3
- Coordinates
- Chromosome 2: 70,777,310–70,790,643 (GRCh38)
- Exons
- 5 exons across 13.3 kb
- Protein
- 219 amino acids
- Also known as
- bHLHc8, Figalpha
- MANE Select transcript
- ENST00000332372.6NM_001004311.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read FIGLA, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Female Infertility
Diminished or absent ability of a female to achieve conception.
- 1 GenCC submitter rates it definitive or strong
How FIGLA is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 0.7 kb of the gene's 13.3 kb; 660 of those bases code for the protein.
How a genome test reads FIGLA
1
position in FIGLA where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 13.3 kb of FIGLA, introns included, not only the 0.7 kb of exons.
Genes linked to the same conditions
- ANKRD31ankyrin repeat domain 31Shares 1 condition
- ATMATM serine/threonine kinaseShares 1 condition
- BMP15bone morphogenetic protein 15Shares 1 condition
- BNC1basonuclin zinc finger protein 1Shares 1 condition
- CLPPcaseinolytic mitochondrial matrix peptidase proteolytic subunitShares 1 condition
- CYP19A1cytochrome P450 family 19 subfamily A member 1Shares 1 condition
- FANCMFA complementation group MShares 1 condition
- FMR1fragile X messenger ribonucleoprotein 1Shares 1 condition
- FOXL2forkhead box L2Shares 1 condition
- FSHRfollicle stimulating hormone receptorShares 1 condition
- GALTgalactose-1-phosphate uridylyltransferaseShares 1 condition
- GDF9growth differentiation factor 9Shares 1 condition
Traits linked to FIGLA
The Human Phenotype Ontology lists these as features of the rare conditions FIGLA can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). FIGLA gene: folliculogenesis specific bHLH transcription factor. Retrieved 16 October 2026, from https://dantelabs.com/genes/figla
Dante Labs. FIGLA gene: folliculogenesis specific bHLH transcription factor [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/figla
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks