Vitamin K metabolism and activation of dependent proteins

Pathway network for the Vitamin K metabolism and activation of dependent proteins SuperPath

Sources:
  • WikiPathways
  • PharmGKB
  • PubChem
  • Reactome

Gene overlap in member pathways for Vitamin K metabolism and activation of dependent proteins SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Vitamin K metabolism and activation of dependent proteins SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hereditary combined deficiency of vitamin k-dependent clotting factorsEnrichmentGGCX, VKORC17.19
2Cerebral sinovenous thrombosisEnrichmentF2, PROZ5.59
3Thrombophilia due to thrombin defectEnrichmentF2, VKORC14.75
4Schnyder corneal dystrophyEnrichmentUBIAD14.13
5Vitamin k-dependent clotting factors, combined deficiency of, 2EnrichmentVKORC13.66
6Congenital vitamin k-dependent coagulation factors deficiencyEnrichmentVKORC13.66
7Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiencyEnrichmentGGCX3.53
8Vitamin k-dependent clotting factors, combined deficiency of, 1EnrichmentGGCX3.53
9Body skin hyperlaxity due to vitamin k-dependent coagulation factor deficiencyEnrichmentGGCX3.53
10Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosaEnrichmentGGCX3.53
11Cerebral palsyEnrichmentF2, PROC3.21
12Coumarin resistanceEnrichmentVKORC13.18
13ThrombocytopeniaEnrichmentF10, PROS13.03
14Thrombophilia due to protein c deficiency, autosomal dominantEnrichmentPROC3.02
15Factor vii deficiencyEnrichmentF73.02
16Warfarin sensitivity, x-linkedEnrichmentF93.02
17Prothrombin deficiency, congenitalEnrichmentF23.02
18Thrombophilia due to protein s deficiency, autosomal dominantEnrichmentPROS13.02
19Thrombophilia due to protein s deficiency, autosomal recessiveEnrichmentPROS13.02
20Protein z deficiencyEnrichmentPROZ3.02
21Thrombophilia, x-linked, due to factor ix defectEnrichmentF93.02
22Thrombophilia due to protein c deficiency, autosomal recessiveEnrichmentPROC3.02
23Pregnancy loss, recurrent 2EnrichmentF23.02
24Protein s deficiencyEnrichmentPROS13.02
25Prothrombin deficiencyEnrichmentF23.02
26Severe hereditary thrombophilia due to congenital protein c deficiencyEnrichmentPROC3.02
27Protein c deficiencyEnrichmentPROC3.02
28Hemophilia b leydenEnrichmentF93.02
29Hereditary thrombophilia due to congenital protein s deficiencyEnrichmentPROS13.02
30Congenital factor vii deficiencyEnrichmentF73.02
31Keutel syndromeEnrichmentMGP2.90
32Genetic lipodystrophyEnrichmentEPHX12.90
33Hemophilia bEnrichmentF92.72
34Factor x deficiencyEnrichmentF102.54
35Congenital factor x deficiencyEnrichmentF102.54
36Hemophilia aEnrichmentF92.42
37Factor viii deficiencyEnrichmentF92.42
38Familial hypercholanemiaEnrichmentEPHX12.13
39Stroke, ischemicEnrichmentF22.02
40Myocardial infarctionEnrichmentF71.68
41Cystic fibrosisEnrichmentEPHX11.40

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