claudin 19, isoform CRA_a [Homo sapiens]

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Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. [J Nephrol. 2021]
Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.
Vall-Palomar M, Burballa C, Claverie-Martín F, Meseguer A, Ariceta G. J Nephrol. 2021 Dec; 34(6):2053-2062. Epub 2021 Apr 30.
Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function. [Commun Biol. 2019]
Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function.
Wang SB, Xu T, Peng S, Singh D, Ghiassi-Nejad M, Adelman RA, Rizzolo LJ. Commun Biol. 2019; 2:113. Epub 2019 Mar 25.
Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutation. [Ophthalmic Genet. 2018]
Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutation.
Khan AO, Patel N, Ghazi NG, Alzahrani SS, Arold ST, Alkuraya FS. Ophthalmic Genet. 2018 Oct; 39(5):577-583. Epub 2018 Aug 1.

RefSeq genomic sequence
See the genomic reference sequence for the CLDN19 gene (NG_008993.1).

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Homologene neighbors for GEO Profiles (Select 90912883) (0)
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Chromosome neighbors for GEO Profiles (Select 90888524) (20)
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Chromosome neighbors for GEO Profiles (Select 90905416) (18)
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Chromosome neighbors for GEO Profiles (Select 90928869) (19)
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BioSample links for Nucleotide (Select 448539122) (1)
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