RecName: Full=Forkhead box protein E3; AltName: Full=Forkhead-related - Protein

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Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans. [Am J Hum Genet. 2006]
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
Valleix S, Niel F, Nedelec B, Algros MP, Schwartz C, Delbosc B, Delpech M, Kantelip B. Am J Hum Genet. 2006 Aug; 79(2):358-64. Epub 2006 Jun 8.
Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease. [Hum Mutat. 2015]
Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease.
Islam L, Kelberman D, Williamson L, Lewis N, Glindzicz MB, Nischal KK, Sowden JC. Hum Mutat. 2015 Mar; 36(3):296-300.
Growth inhibition of human lens epithelial cells by short hairpin RNA in transcription factor forkhead box E3 (FOXE3). [Graefes Arch Clin Exp Ophthalm...]
Growth inhibition of human lens epithelial cells by short hairpin RNA in transcription factor forkhead box E3 (FOXE3).
Wang Y, Li W, Wang Y, Huang Y. Graefes Arch Clin Exp Ophthalmol. 2012 Jul; 250(7):999-1007. Epub 2012 Apr 18.

RefSeq protein
See the reference protein sequence for forkhead box protein E3 (NP_599166.1).

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RecName: Full=Forkhead box protein E3; AltName: Full=Forkhead-related protein FK...
RecName: Full=Forkhead box protein E3; AltName: Full=Forkhead-related protein FKHL12; AltName: Full=Forkhead-related transcription factor 8; Short=FREAC-8; AltName: Full=Hepatocyte nuclear factor 3 forkhead homolog 7; Short=HFH-7
gi|857434439|sp|Q63250.2|FOXE3_RAT

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