Osteopontin signaling

No Pathway Network information available for Osteopontin signaling

Pathways in the Osteopontin signaling SuperPath

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

Disorders associated with Osteopontin signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melorheostosis, isolatedEnrichmentMAP2K13.02
2Cardiofaciocutaneous syndrome 3EnrichmentMAP2K13.02
3Fetal encasement syndromeEnrichmentCHUK3.02
4Immunodeficiency 15bEnrichmentIKBKB3.02
5Noonan syndrome 13EnrichmentMAPK13.02
6Immunodeficiency 15aEnrichmentIKBKB3.02
7MelorheostosisEnrichmentMAP2K13.02
8Bartsocas-papas syndrome 2EnrichmentCHUK3.02
9Immunodeficiency 112EnrichmentMAP3K143.02
10Immune dysregulation, neurodevelopmental defects, and colitisEnrichmentITGAV3.02
11Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK3.02
12Nik deficiencyEnrichmentMAP3K143.02
13Quebec platelet disorderEnrichmentPLAU2.72
14Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.72
15Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.72
16Rela fusion-positive ependymomaEnrichmentRELA2.72
17Metaphyseal anadysplasia 2EnrichmentMMP92.72
18Metaphyseal anadysplasiaEnrichmentMMP92.72
19Common variable immunodeficiency 12EnrichmentNFKB12.72
20Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentITGB32.54
21Bleeding disorder, platelet-type, 16EnrichmentITGB32.54
22Langerhans cell histiocytosisEnrichmentMAP2K12.54
23Bleeding disorder, platelet-type, 24EnrichmentITGB32.54
24Cardiofaciocutaneous syndrome 1EnrichmentMAP2K12.42
25Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.42
26Cardiofaciocutaneous syndromeEnrichmentMAP2K12.42
27Pediatric systemic lupus erythematosusEnrichmentSPP12.42
28Alzheimer disease 2EnrichmentPLAU2.32
29Glanzmann thrombasthenia 2EnrichmentITGB32.32
30Fetomaternal alloimmune thrombocytopenia 1EnrichmentITGB32.24
31Glanzmann thrombasthenia 1EnrichmentITGB32.17
32Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K12.17
33Common variable immunodeficiencyEnrichmentNFKB12.17
34Arteriovenous malformationEnrichmentMAP2K12.07
35Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K12.02
36Ciliary dyskinesia, primary, 3EnrichmentNFKB12.02
37Autosomal dominant macrothrombocytopeniaEnrichmentITGB32.02
38Lung non-small cell carcinomaEnrichmentMAP2K11.98
39Specific learning disabilityEnrichmentMAPK11.98
40Noonan syndrome and noonan-related syndromeEnrichmentMAP2K11.85
41Alzheimer disease, familial, 1EnrichmentPLAU1.79
42Heart, malformation ofEnrichmentMAPK11.77
43Myocardial infarctionEnrichmentITGB31.68
44Noonan syndrome 1EnrichmentMAP2K11.66
45RasopathyEnrichmentMAP2K11.61
46Severe covid-19EnrichmentITGAV1.56
47Severe combined immunodeficiencyEnrichmentIKBKB1.51
48Systemic lupus erythematosusEnrichmentSPP11.43
49ThrombocytopeniaEnrichmentITGB31.35
50Autism spectrum disorderEnrichmentMAP2K11.00
51MicrocephalyEnrichmentMAPK10.95

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