KIAA1773 protein [Homo sapiens]

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Mutation in mitral valve prolapse susceptible gene DCHS1 causes familial mitral annular disjunction. [J Med Genet. 2024]
Mutation in mitral valve prolapse susceptible gene DCHS1 causes familial mitral annular disjunction.
Zhou N, Zhao Q, Li R, Cheng R, Wu Q, Cheng J, Chen Y. J Med Genet. 2024 Jan 19; 61(2):125-131. Epub 2024 Jan 19.
De novo DCHS1 splicing mutation in a patient with mitral valve prolapse. [QJM. 2023]
De novo DCHS1 splicing mutation in a patient with mitral valve prolapse.
Li D, Yi Z, Wu Q, Huang Y, Yao H, Tan Z, Yang Y, Zhang W. QJM. 2023 Feb 24; 116(2):121-122.
DCHS1 DNA copy number loss associated with pediatric urinary tract infection risk. [Innate Immun. 2020]
DCHS1 DNA copy number loss associated with pediatric urinary tract infection risk.
Qureshi AH, Liang D, Canas J, Hooks J, Arrregui SW, Saxena V, Rooney R, Nolan V, Schwaderer AL, Hains DS. Innate Immun. 2020 Aug; 26(6):473-481. Epub 2020 Apr 15.

RefSeq genomic sequence
See the genomic reference sequence for the DCHS1 gene (NG_033858.2).
RefSeq protein
See the reference protein sequence for protocadherin-16 precursor (NP_003728.1).

Nucleotide
Nucleotide sequence from coding region
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Rattus norvegicus Cd47 molecule (Cd47), mRNA
Rattus norvegicus Cd47 molecule (Cd47), mRNA
gi|55742751|ref|NM_019195.2|

Nucleotide

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Protein