RecName: Full=Myosin-14; AltName: Full=Myosin heavy chain 14; AltName: - Protein

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Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. [Am J Med Genet A. 2024]
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.
Duman D, Ramzan M, Subasioglu A, Mutlu A, Peart L, Seyhan S, Guo S, Ila K, Balta B, Kalcioglu MT, et al. Am J Med Genet A. 2024 Jun; 194(6):e63563. Epub 2024 Feb 14.
Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants. [Genes (Basel). 2021]
Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants.
Hiramatsu K, Nishio SY, Kitajiri SI, Kitano T, Moteki H, Usami SI, On Behalf Of The Deafness Gene Study Consortium. Genes (Basel). 2021 Oct 15; 12(10). Epub 2021 Oct 15.
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss. [BMC Med Genet. 2020]
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss.
Wang M, Zhou Y, Zhang F, Fan Z, Bai X, Wang H. BMC Med Genet. 2020 Jul 25; 21(1):154. Epub 2020 Jul 25.

RefSeq genomic sequence
See the genomic reference sequence for the MYH14 gene (NG_011645.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the MYH14 gene.

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Q7Z406 [Domain Mapping of Disease Mut...]
Q7Z406
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
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reagent reviews [ExactAntigen/Labome]
reagent reviews
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Protein