RecName: Full=Factor in the germline alpha; Short=FIGalpha; AltName: F - Protein

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Bi-allelic recessive loss-of-function mutations in FIGLA cause premature ovarian insufficiency with short stature. [Clin Genet. 2019]
Bi-allelic recessive loss-of-function mutations in FIGLA cause premature ovarian insufficiency with short stature.
Yuan P, He Z, Sun S, Li Y, Wang W, Liang X, Xie X, Jiang Y, Yang D. Clin Genet. 2019 Mar; 95(3):409-414. Epub 2018 Dec 18.
Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency. [J Ovarian Res. 2018]
Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.
Chen B, Li L, Wang J, Li T, Pan H, Liu B, Zhou Y, Cao Y, Wang B. J Ovarian Res. 2018 Jun 18; 11(1):48. Epub 2018 Jun 18.
Mutational analysis of the FIGLA gene in women with idiopathic premature ovarian failure. [Menopause. 2015]
Mutational analysis of the FIGLA gene in women with idiopathic premature ovarian failure.
Tosh D, Rani HS, Murty US, Deenadayal A, Grover P. Menopause. 2015 May; 22(5):520-6.

RefSeq genomic sequence
See the genomic reference sequence for the FIGLA gene (NG_013044.1).
RefSeq protein
See the reference protein sequence for factor in the germline alpha (NP_001004311.2).

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Q6QHK4 [Domain Mapping of Disease Mut...]
Q6QHK4
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Factor in the germline alpha; Short=FIGalpha; AltName: Full=Class ...
RecName: Full=Factor in the germline alpha; Short=FIGalpha; AltName: Full=Class C basic helix-loop-helix protein 8; Short=bHLHc8; AltName: Full=Folliculogenesis-specific basic helix-loop-helix protein; AltName: Full=Transcription factor FIGa
gi|296434505|sp|Q6QHK4.2|FIGLA_HUMA

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