claudin-14 isoform X1 [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 (XM_047440736.1).
RefSeq protein isoforms
See 8 reference sequence protein isoforms for the CLDN14 gene.

claudin-14 isoform X1 [Homo sapiens]
claudin-14 isoform X1 [Homo sapiens]
gi|2217337492|ref|XP_047296692.1|

Protein
histidine--tRNA ligase, cytoplasmic isoform 5 [Homo sapiens]
histidine--tRNA ligase, cytoplasmic isoform 5 [Homo sapiens]
gi|574278766|ref|NP_001276021.1|

Protein
Eyelids
Eyelids
Each of the upper and lower folds of SKIN which cover the EYE when closed.<br/>

MeSH
Product Line Management
Product Line Management
Management control systems for structuring health care delivery strategies around case types, as in DRGs, or specific clinical services.<br/>Year introduced: 1991(1988)

MeSH
Genetic Phenomena
Genetic Phenomena
The biological processes, properties, and objects that are involved in maintaining, expressing, and transmitting from one organism to another, genetically encoded traits....<br/>Year introduced: 2009

MeSH

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Protein