otoancorin isoform 1 precursor [Homo sapiens]

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[Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations]. [Zhonghua Er Bi Yan Hou Tou Jin...]
[Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations].
Yang JY, Wang QQ, Han MY, Huang SS, Kang DY, Zhang X, Yang SY, Dai P, Yuan YY. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023 May 7; 58(5):460-469.
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients. [Hum Mutat. 2021]
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients.
Laurent S, Gehrig C, Nouspikel T, Amr SS, Oza A, Murphy E, Vannier A, Béna FS, Carminho-Rodrigues MT, Blouin JL, et al. Hum Mutat. 2021 Apr; 42(4):373-377. Epub 2021 Mar 14.
Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness. [Hum Mutat. 2019]
Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness.
Kim BJ, Kim DK, Han JH, Oh J, Kim AR, Lee C, Kim NK, Park HR, Kim MY, Lee S, et al. Hum Mutat. 2019 May; 40(5):525-531. Epub 2019 Feb 28.

RefSeq genomic sequence
See the genomic reference sequence for the OTOA gene (NG_012973.2).
RefSeq mRNA
See reference mRNA sequence for the OTOA gene (NM_144672.4).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the OTOA gene.

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Protein