Homo sapiens cadherin related 23 (CDH23), transcript variant 1, mRNA

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Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants. [Sci Rep. 2024]
Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants.
Tsukada K, Nishio SY, Takumi Y, Usami SI. Sci Rep. 2024 May 8; 14(1):10596. Epub 2024 May 8.
Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population. [Genet Test Mol Biomarkers. 2024]
Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population.
Tang X, Cheng H, Cheng L, Liang B, Chen M, Zheng X, Xiao F. Genet Test Mol Biomarkers. 2024 Mar; 28(3):123-130.
A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation. [Audiol Neurootol. 2023]
A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation.
Khorram E, Iravani O, Khorrami M, Amini M, Jahanian S, Nilforoush MH, Mousavi SR, Ehsanifard M, Kheirollahi M. Audiol Neurootol. 2023; 28(4):317-326. Epub 2023 Apr 21.

RefSeq protein product
See the reference protein sequence for cadherin-23 isoform 1 precursor (NP_071407.4).

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
CCDS
Link to Consensus CDS
Components (Core)
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Full text in PMC
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Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
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Homo sapiens cadherin related 23 (CDH23), transcript variant 1, mRNA
Homo sapiens cadherin related 23 (CDH23), transcript variant 1, mRNA
gi|1653962144|ref|NM_022124.6|

Nucleotide
Progressive sclerosing poliodystrophy
Progressive sclerosing poliodystrophy

MedGen
"Generalized non-convulsive status epilepticus without coma"[Clin... (2)
"Generalized non-convulsive status epilepticus without coma"[Clinical Features] OR 124372[uid]
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MedGen
"Aciduria"[Clinical Features] OR 488840[uid] (3)
MedGen
PMC Articles for MedGen (Select 489988) (4)
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Nucleotide