Homo sapiens complement factor H related 3 (CFHR3), transcript variant - Nucleotide

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Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication. [Front Immunol. 2024]
Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication.
Tasaki Y, Tsujimoto H, Yokoyama T, Sugimoto N, Kitajima S, Fujii H, Hidaka Y, Kato N, Maruyama S, Inoue N, et al. Front Immunol. 2024; 15:1360855. Epub 2024 Mar 8.
The absence of CFHR3 and CFHR1 genes from the T2T-CHM13 assembly can limit the molecular diagnosis of complement-related diseases. [Eur J Hum Genet. 2023]
The absence of CFHR3 and CFHR1 genes from the T2T-CHM13 assembly can limit the molecular diagnosis of complement-related diseases.
Hamza A, El-Sissy C, Yousfi N, Martins PV, Rafat C, Masliah-Planchon J, Frémeaux-Bacchi V, Mesnard L. Eur J Hum Genet. 2023 Jul; 31(7):730-732. Epub 2023 Apr 10.
CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome. [Front Immunol. 2022]
CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome.
Piras R, Valoti E, Alberti M, Bresin E, Mele C, Breno M, Liguori L, Donadelli R, Rigoldi M, Benigni A, et al. Front Immunol. 2022; 13:1011580. Epub 2023 Jan 30.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the CFHR3 gene (NM_001166624.2).
RefSeq protein product
See the reference protein sequence for complement factor H-related protein 3 isoform 1 precursor (NP_066303.2).

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Homo sapiens complement factor H related 3 (CFHR3), transcript variant 1, mRNA
Homo sapiens complement factor H related 3 (CFHR3), transcript variant 1, mRNA
gi|1780222577|ref|NM_021023.6|

Nucleotide

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Nucleotide