Homo sapiens complement factor I (CFI), transcript variant 9, mRNA

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Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome. [Am J Kidney Dis. 2024]
Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome.
Schwotzer N, Fakhouri F, Martins PV, Delmas Y, Caillard S, Zuber J, Moranne O, Mesnard L, Frémeaux-Bacchi V, El-Sissy C. Am J Kidney Dis. 2024 Aug; 84(2):244-249. Epub 2024 Feb 28.
Elevated expression of complement factor I in lung cancer cells associates with shorter survival-Potentially via non-canonical mechanism. [Transl Res. 2024]
Elevated expression of complement factor I in lung cancer cells associates with shorter survival-Potentially via non-canonical mechanism.
Felberg A, Bieńkowski M, Stokowy T, Myszczyński K, Polakiewicz Z, Kitowska K, Sądej R, Mohlin F, Kuźniewska A, Kowalska D, et al. Transl Res. 2024 Jul; 269:1-13. Epub 2024 Feb 22.
CNS Inflammation as the First Sign of Complement Factor I Deficiency: A Severe Myelitis Treated With Intense Immunotherapy and Eculizumab. [Neurol Neuroimmunol Neuroinfla...]
CNS Inflammation as the First Sign of Complement Factor I Deficiency: A Severe Myelitis Treated With Intense Immunotherapy and Eculizumab.
Massey V, Nguyen CE, François T, De Bruycker JJ, Bonnefoy A, Lapeyraque AL, Decaluwe H. Neurol Neuroimmunol Neuroinflamm. 2024 Mar; 11(2):e200191. Epub 2023 Dec 22.

RefSeq alternative splicing
See 23 reference mRNA sequence splice variants for the CFI gene.
RefSeq protein product
See the reference protein sequence for complement factor I isoform 9 preproprotein (NP_001362212.1).

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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Gene
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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