Homo sapiens complement factor H-related 3, mRNA (cDNA clone MGC:61905 - 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 2 reference mRNA sequence splice variants for the CFHR3 gene.

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Nucleotide