Homo sapiens complement C2 (C2), RefSeqGene (LRG_26) on chromosome 6

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Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein. [Mol Cell Proteomics. 2023]
Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein.
Burnap SA, Ortega-Prieto AM, Jimenez-Guardeño JM, Ali H, Takov K, Fish M, Shankar-Hari M, Giacca M, Malim MH, Mayr M. Mol Cell Proteomics. 2023 Aug; 22(8):100600. Epub 2023 Jun 19.
Defective microbial sensing and clearance in perianal Crohn's disease: a role for complement factor B. [Gut. 2023]
Defective microbial sensing and clearance in perianal Crohn's disease: a role for complement factor B.
Ghate A, Uhlig HH. Gut. 2023 Nov; 72(11):2010-2012. Epub 2023 Apr 25.
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis. [Gut. 2023]
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis.
Akhlaghpour M, Haritunians T, More SK, Thomas LS, Stamps DT, Dube S, Li D, Yang S, Landers CJ, Mengesha E, et al. Gut. 2023 Nov; 72(11):2068-2080. Epub 2023 Apr 20.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the C2 gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.
SNP
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3D structures for Gene (Select 717) (5)
Structure
Homo sapiens tenascin XB (TNXB), transcript variant 3, mRNA
Homo sapiens tenascin XB (TNXB), transcript variant 3, mRNA
gi|1653961980|ref|NM_001365276.2|

Nucleotide

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Nucleotide