Homo sapiens claudin 16 (CLDN16), transcript variant 2, mRNA

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A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family. [Iran J Kidney Dis. 2022]
A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family.
Malakoutian T, Madadi B, Saber S. Iran J Kidney Dis. 2022 May; 16(3):209-213.
In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria. [Medicina (Kaunas). 2019]
In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria.
Rouka E, Liakopoulos V, Gourgoulianis KI, Hatzoglou C, Zarogiannis SG. Medicina (Kaunas). 2019 Jul 26; 55(8). Epub 2019 Jul 26.
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations. [BMC Med Genet. 2019]
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations.
Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L, Claverie-Martin F. BMC Med Genet. 2019 Jan 8; 20(1):6. Epub 2019 Jan 8.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the CLDN16 gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
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Components (Core)
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Gene
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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gi|2270219366|gb|UTI93290.1|

Protein
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Nucleotide
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Nucleotide
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Nucleotide

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Nucleotide