F8 - coagulation factor VIII Gene

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 302470

Summary

Predicted to enable copper ion binding activity and oxidoreductase activity. Involved in blood coagulation, intrinsic pathway. Located in extracellular space. Used to study Factor VIII deficiency; hemarthrosis; and hyperhomocysteinemia. Human ortholog(s) of this gene implicated in Factor VIII deficiency. Orthologous to human F8 (coagulation Factor VIII). [provided by Alliance of Genome Resources, Apr 2022]

F8 Products (1)

mRNA Protein Name
NM_183331.2 NP_899160.2 coagulation factor VIII precursor
Biological Process GO Annotation Evidence References Source
involved in blood coagulation, intrinsic pathway IMP
IMP: Inferred from mutant phenotype
2513867 RGD
Cellular Component GO Annotation Evidence References Source
located in extracellular space IDA
IDA: Inferred from direct assay
2513867 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

coagulation factor VIII

  • coagulation factor VIII, procoagulant component

Orthologs Information

Species Symbol Source ID
Homo sapiens F8 NCBI NCBI:2157