Signal regulatory protein family interactions

No Pathway Network information available for Signal regulatory protein family interactions

Pathways in the Signal regulatory protein family interactions SuperPath

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

Disorders associated with Signal regulatory protein family interactions SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Interstitial lung disease 2EnrichmentSFTPA1, SFTPA23.76
2MetachondromatosisEnrichmentPTPN112.93
3Leopard syndrome 1EnrichmentPTPN112.93
4Interstitial lung disease 1EnrichmentSFTPA12.93
5Thrombocytopenia 3EnrichmentFYB12.93
6Thrombocytopenia 6EnrichmentSRC2.93
7Congenital autosomal recessive small-platelet thrombocytopeniaEnrichmentFYB12.93
8Vegetative pyoderma gangrenosumEnrichmentPTPN62.93
9Bullous pyoderma gangrenosumEnrichmentPTPN62.93
10Pustular pyoderma gangrenosumEnrichmentPTPN62.93
11Classic pyoderma gangrenosumEnrichmentPTPN62.93
12Malignant astrocytomaEnrichmentPTPN112.93
13ThrombocytopeniaEnrichmentPTPN11, SRC2.85
14Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1EnrichmentTYROBP2.63
15Werner syndromeEnrichmentPTPN112.63
16Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.45
17Tricuspid valve insufficiencyEnrichmentPTPN112.45
18Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.33
19Noonan syndrome with multiple lentiginesEnrichmentPTPN112.33
20LymphomaEnrichmentPTPN112.23
21Patent ductus arteriosusEnrichmentPTPN112.15
22MyelofibrosisEnrichmentSRC2.08
23Noonan syndrome 3EnrichmentPTPN112.08
24Pectus excavatumEnrichmentPTPN111.89
25Specific learning disabilityEnrichmentPTPN111.89
26EpicanthusEnrichmentPTPN111.85
27Juvenile myelomonocytic leukemiaEnrichmentPTPN111.85
28Congenital long qt syndromeEnrichmentPTPN111.85
29OsteoporosisEnrichmentSRC1.79
30Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.76
31Patent foramen ovaleEnrichmentPTPN111.68
32Noonan syndrome 1EnrichmentPTPN111.57
33ScoliosisEnrichmentPTPN111.55
34Hydrops fetalis, nonimmuneEnrichmentPTPN111.52
35RasopathyEnrichmentPTPN111.52
36StrabismusEnrichmentPTPN111.50
37Long qt syndrome 1EnrichmentPTPN111.46
38Non-immune hydrops fetalisEnrichmentPTPN111.44
39Hypertrophic cardiomyopathyEnrichmentPTPN111.30
40Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.19
41Colorectal cancerEnrichmentSRC1.01
42Autism spectrum disorderEnrichmentPTPN110.92
43MicrocephalyEnrichmentPTPN110.87
44Inherited cancer-predisposing syndromeEnrichmentPTPN110.84

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