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
Pyroglutamyl-Peptidase I
Pyroglutamyl-Peptidase I
An enzyme that catalyzes the release of a N-terminal pyroglutamyl group from a polypeptide provided the next residue is not proline. It is inhibited by thiol-blocking reagents...<br/>Year introduced: 1995: was 2005-OXOPROLYL-PEPTIDASE 1991-1994

MeSH
Deoxyribonuclease EcoRI
Deoxyribonuclease EcoRI
One of the Type II site-specific deoxyribonucleases (EC 3.1.21.4). It recognizes and cleaves the sequence G/AATTC at the slash. EcoRI is from E coliRY13. Several isoschizomers...<br/>Year introduced: 1989

MeSH

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Protein