tectorin alpha, isoform CRA_b [Homo sapiens]

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Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. [Hum Mutat. 2022]
Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.
Chen R, Diaz-Miranda MA, Aref-Eshghi E, Hartman TR, Griffith C, Morrison JL, Wheeler PG, Torti E, Richard G, Kenna M, et al. Hum Mutat. 2022 Dec; 43(12):1837-1843. Epub 2022 Aug 2.
[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene].
Zhou C, Li S, Song Q, Liu X, Miao Z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10; 36(2):147-150.
Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. [Orphanet J Rare Dis. 2017]
Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.
Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, et al. Orphanet J Rare Dis. 2017 Sep 25; 12(1):157. Epub 2017 Sep 25.

RefSeq genomic sequence
See the genomic reference sequence for the TECTA gene (NG_011633.1).
RefSeq protein
See the reference protein sequence for alpha-tectorin precursor (NP_005413.2).

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