POU domain, class 3, transcription factor 2 [Homo sapiens]

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Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene's candidacy in 6q16.1 deletions. [Am J Hum Genet. 2023]
Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene's candidacy in 6q16.1 deletions.
Schönauer R, Jin W, Findeisen C, Valenzuela I, Devlin LA, Murrell J, Bedoukian EC, Pöschla L, Hantmann E, Riedhammer KM, et al. Am J Hum Genet. 2023 Jun 1; 110(6):998-1007. Epub 2023 May 18.
Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder. [PLoS Genet. 2021]
Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder.
Huang K, Wu Y, Shin J, Zheng Y, Siahpirani AF, Lin Y, Ni Z, Chen J, You J, Keles S, et al. PLoS Genet. 2021 Feb; 17(2):e1009309. Epub 2021 Feb 4.
Unexpected High Levels of BRN2/POU3F2 Expression in Human Dermal Melanocytic Nevi. [J Invest Dermatol. 2020]
Unexpected High Levels of BRN2/POU3F2 Expression in Human Dermal Melanocytic Nevi.
Chitsazan A, Lambie D, Ferguson B, Handoko HY, Gabrielli B, Walker GJ, Boyle GM. J Invest Dermatol. 2020 Jun; 140(6):1299-1302.e4. Epub 2019 Dec 24.

RefSeq protein
See the reference protein sequence for POU domain, class 3, transcription factor 2 (NP_005595.2).

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reagents [ExactAntigen/Labome]
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