Homo sapiens POU class 3 homeobox 4 (POU3F4), RefSeqGene on chromosome - Nucleotide

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Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes. [Am J Med Genet A. 2024]
Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes.
Chandrasekhar A, Mroczkowski HJ, Urraca N, Gross A, Bluske K, Thorpe E, Hagelstrom RT, Schonberg SA, Perry DL, Taft RJ, et al. Am J Med Genet A. 2024 Mar; 194(3):e63462. Epub 2023 Nov 6.
REST Inactivation and Coexpression of ASCL1 and POU3F4 Are Necessary for the Complete Transformation of RB1/TP53-Inactivated Lung Adenocarcinoma into Neuroendocrine Carcinoma. [Am J Pathol. 2022]
REST Inactivation and Coexpression of ASCL1 and POU3F4 Are Necessary for the Complete Transformation of RB1/TP53-Inactivated Lung Adenocarcinoma into Neuroendocrine Carcinoma.
Masawa M, Sato-Yazawa H, Kashiwagi K, Ishii J, Miyata-Hiramatsu C, Iwamoto M, Kohno K, Miyazawa T, Onozaki M, Noda S, et al. Am J Pathol. 2022 Jun; 192(6):847-861. Epub 2022 Mar 30.
X-linked Malformation Deafness: Neurodevelopmental Symptoms Are Common in Children With IP3 Malformation and Mutation in POU3F4. [Ear Hear. 2022]
X-linked Malformation Deafness: Neurodevelopmental Symptoms Are Common in Children With IP3 Malformation and Mutation in POU3F4.
Smeds H, Wales J, Karltorp E, Anderlid BM, Henricson C, Asp F, Anmyr L, Lagerstedt-Robinson K, Löfkvist U. Ear Hear. 2022 Jan/Feb; 43(1):53-69.

Protein
Protein sequence from Nucleotide coding region
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protocadherin-11 X-linked isoform X4 [Homo sapiens]
protocadherin-11 X-linked isoform X4 [Homo sapiens]
gi|2462629012|ref|XP_054182817.1|

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Nucleotide