Gene table of F5 : coagulation factor V

Gene-disease associations table

Disease IDDisease nameSource of annotation with F5OMIM linkNumber of associated genesgenes
614389PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1ClinVar, OMIM link to OMIM 1F5
227400FACTOR V DEFICIENCYClinVar, OMIM, HUMSAVAR link to OMIM 1F5
600880BUDD-CHIARI SYNDROMEOMIM link to OMIM 1F5
601367STROKE, ISCHEMICOMIM link to OMIM 5PRKCH, NOS3, ALOX5AP, F5, F2
PS188050THROMBOPHILIAClinVar, OMIM, HUMSAVAR link to OMIM 13HRG, SERPIND1, F5, MTHFR, SERPINC1, THBD, F2, PROS1, PLAT, F9, HABP2, F13A1, PROC

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Annotation of the gene F5

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
KEGG pathwayKEGG IDKEGG IC
Complement and coagulation cascadeshsa046106.58
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
Platelet degranulation R-HSA-1146086.68
Platelet activation, signaling and aggregationR-HSA-760025.15
Response to elevated platelet cytosolic Ca2+R-HSA-760056.59
Common Pathway of Fibrin Clot FormationR-HSA-1408758.52
Formation of Fibrin Clot (Clotting Cascade)R-HSA-1408777.7
HemostasisR-HSA-1095823.98
Associated GO terms for Molecular function
GO termGO IDGO IC
cation bindingGO:00431691.4
copper ion bindingGO:00055075.71
transition metal ion bindingGO:00469142.48
ion bindingGO:00431671.36
bindingGO:00054880.18
protein bindingGO:00055150.46
metal ion bindingGO:00468721.41