G-protein signaling_Regulation of CDC42 activity

No Pathway Network information available for G-protein signaling_Regulation of CDC42 activity

Pathways in the G-protein signaling_Regulation of CDC42 activity SuperPath

#NameSourceGenes
1G-protein signaling_Regulation of CDC42 activityGeneGo (Thomson Reuters)

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

Disorders associated with G-protein signaling_Regulation of CDC42 activity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Adams-oliver syndrome 1EnrichmentARHGAP31, DOCK64.79
2Chromosome 8p11 myeloproliferative syndromeEnrichmentBCR, FGFR14.79
3Adams-oliver syndromeEnrichmentARHGAP31, DOCK63.95
4Osteoglophonic dysplasiaEnrichmentFGFR12.63
5Cystic angiomatosis of bone, diffuseEnrichmentRASA12.63
6Trigonocephaly 1EnrichmentFGFR12.63
7Autoinflammatory disease, multisystem, with immune dysregulation, x-linkedEnrichmentDOCK112.63
8Nephrotic syndrome, type 8EnrichmentARHGDIA2.63
9Charcot-marie-tooth disease, demyelinating, type 4hEnrichmentFGD42.63
10Immunodeficiency 87 and autoimmunityEnrichmentDEF62.63
11Charcot-marie-tooth disease type 4hEnrichmentFGD42.63
12Hartsfield syndromeEnrichmentFGFR12.63
13Takenouchi-kosaki syndromeEnrichmentCDC422.63
14Infantile-onset mesial temporal lobe epilepsy with severe cognitive regressionEnrichmentTNK22.63
15Gorham's diseaseEnrichmentRASA12.63
16Nocarh syndromeEnrichmentCDC422.63
17Hartsfield-bixler-demyer syndromeEnrichmentFGFR12.63
18Pfeiffer syndromeEnrichmentFGFR12.33
19Jackson-weiss syndromeEnrichmentFGFR12.33
20Encephalocraniocutaneous lipomatosisEnrichmentFGFR12.33
21Adams-oliver syndrome 2EnrichmentDOCK62.33
22Rosette-forming glioneuronal tumorEnrichmentFGFR12.33
23Immune system diseaseEnrichmentCDC422.33
24Paget's disease of boneEnrichmentDOCK62.33
25Aarskog syndromeEnrichmentFGD12.33
26Interfrontal craniofaciosynostosisEnrichmentFGFR12.33
27Hypogonadotropic hypogonadism 2 with or without anosmiaEnrichmentFGFR12.15
28Aarskog-scott syndromeEnrichmentFGD12.15
29Intellectual developmental disorder, x-linked, syndromic, claes-jensen typeEnrichmentFGD12.15
30Hypercholanemia, familial 1EnrichmentDOCK62.15
31Wieacker-wolff syndromeEnrichmentRASA12.15
32Syndromic x-linked intellectual disability claes-jensen typeEnrichmentFGD12.15
33Chromosome 22q11.2 deletion syndrome, distalEnrichmentBCR2.03
34Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC422.03
35Capillary malformations, congenitalEnrichmentRASA11.93
36Martsolf syndrome 1EnrichmentARHGAP51.93
37HoloprosencephalyEnrichmentFGFR11.93
38Primary hypereosinophilic syndromeEnrichmentFGFR11.93
39Klippel-trenaunay-weber syndromeEnrichmentRASA11.85
40Telangiectasia, hereditary hemorrhagic, type 1EnrichmentRASA11.85
41Holoprosencephaly 1EnrichmentFGFR11.85
42Hemangioma, capillary infantileEnrichmentRASA11.85
43Basal cell carcinoma 1EnrichmentRASA11.85
44Capillary malformation-arteriovenous malformation 1EnrichmentRASA11.79
45Leukemia, chronic myeloidEnrichmentBCR1.79
46Hereditary hemorrhagic telangiectasiaEnrichmentRASA11.79
47Pilomyxoid astrocytomaEnrichmentFGFR11.79
48B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentBCR1.79
49Arteriovenous malformationEnrichmentRASA11.68
50Hypogonadotropic hypogonadismEnrichmentFGFR11.68
51Myopathy, x-linked, with excessive autophagyEnrichmentRASA11.63
52Septooptic dysplasiaEnrichmentFGFR11.55
53Hypercholesterolemia, familial, 1EnrichmentDOCK61.52
54Neural tube defectsEnrichmentDLC11.52
55Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentFGFR11.49
56Familial hypercholesterolemiaEnrichmentDOCK61.46
57GliosarcomaEnrichmentFGFR11.43
58Microform holoprosencephalyEnrichmentFGFR11.43
59Lobar holoprosencephalyEnrichmentFGFR11.43
60Giant cell glioblastomaEnrichmentFGFR11.40
61Charcot-marie-tooth disease type 4EnrichmentFGD41.38
62Semilobar holoprosencephalyEnrichmentFGFR11.38
63Normosmic congenital hypogonadotropic hypogonadismEnrichmentFGFR11.38
64Parkinson's diseaseEnrichmentTNK21.36
65Tooth agenesisEnrichmentFGFR11.30
66Kallmann syndromeEnrichmentFGFR11.28
67Precursor t-cell acute lymphoblastic leukemiaEnrichmentBCR1.28
68Genetic steroid-resistant nephrotic syndromeEnrichmentARHGDIA1.11
69Cerebral palsyEnrichmentARHGAP311.05
70Autosomal recessive non-syndromic intellectual disabilityEnrichmentEZR0.89
71Colorectal cancerEnrichmentDLC10.73

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