claudin-14 [Homo sapiens]

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Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant. [Int J Mol Sci. 2019]
Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.
Kitano T, Kitajiri SI, Nishio SY, Usami SI. Int J Mol Sci. 2019 Sep 16; 20(18). Epub 2019 Sep 16.
Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss. [Int J Pediatr Otorhinolaryngol...]
Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.
Lu Y, Yao J, Wei Q, Xu J, Xing G, Cao X. Int J Pediatr Otorhinolaryngol. 2018 Feb; 105:6-11. Epub 2017 Nov 22.
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect. [Hum Genet. 2017]
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.
Pater JA, Benteau T, Griffin A, Penney C, Stanton SG, Predham S, Kielley B, Squires J, Zhou J, Li Q, et al. Hum Genet. 2017 Jan; 136(1):107-118. Epub 2016 Nov 12.

RefSeq genomic sequence
See the genomic reference sequence for the CLDN14 gene (NG_011777.1).
RefSeq mRNA
See reference mRNA sequence for the CLDN14 gene (NM_001146077.2).

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NP_001139549 [Domain Mapping of Disease Mut...]
NP_001139549
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
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