Cfb - complement factor B Gene

Also Known as Bf; Da1-24

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 294257

Summary

Predicted to enable G protein-coupled receptor activity and serine-type endopeptidase activity. Involved in complement activation; response to lipopolysaccharide; and response to thyroid hormone. Located in extracellular space. Biomarker of polycystic kidney disease and retinal degeneration. Human ortholog(s) of this gene implicated in several diseases, including atypical hemolytic-uremic syndrome; autoimmune disease (multiple); eye disease (multiple); glomerulonephritis (multiple); and sickle cell anemia. Orthologous to human CFB (Complement Factor B). [provided by Alliance of Genome Resources, Apr 2022]

Cfb Products (1)

mRNA Protein Name
NM_212466.3 NP_997631.2 complement factor B precursor
Biological Process GO Annotation Evidence References Source
involved in complement activation IDA
IDA: Inferred from direct assay
6906329 RGD
involved in response to lipopolysaccharide IEP
IEP: Inferred from expression pattern
18023983 RGD
involved in response to thyroid hormone IMP
IMP: Inferred from mutant phenotype
22370704 RGD
Cellular Component GO Annotation Evidence References Source
located in extracellular space IDA
IDA: Inferred from direct assay
3853462 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

complement factor B

  • B-factor, properdin

  • properdin factor B

Orthologs Information

Species Symbol Source ID
Homo sapiens Cfb NCBI NCBI:629