G-protein signaling_Regulation of RAC1 activity

No Pathway Network information available for G-protein signaling_Regulation of RAC1 activity

Pathways in the G-protein signaling_Regulation of RAC1 activity SuperPath

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

Disorders associated with G-protein signaling_Regulation of RAC1 activity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E7.38
2Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G, ZAP707.01
3Immunodeficiency 7EnrichmentTRA, TRAC4.44
4Precursor t-cell acute lymphoblastic leukemiaEnrichmentBCR, TRA, TRB4.15
5Nephrotic syndrome, type 8EnrichmentARHGDIA2.45
6Immunodeficiency 87 and autoimmunityEnrichmentDEF62.45
7Neurodevelopmental disorder with midbrain and hindbrain malformationsEnrichmentARHGEF22.45
8Immunodeficiency 81EnrichmentLCP22.45
9Immunodeficiency 48EnrichmentZAP702.45
10Immunodeficiency 18EnrichmentCD3E2.45
11Immunodeficiency 25EnrichmentCD2472.45
12Immunodeficiency, common variable, 3EnrichmentCD192.45
13Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.45
14Alfadhel syndromeEnrichmentRAP1GDS12.45
15Neurodevelopmental disorder with language delay and seizuresEnrichmentTIAM12.45
16Infantile-onset mesial temporal lobe epilepsy with severe cognitive regressionEnrichmentTNK22.45
17Immunodeficiency 19, severe combinedEnrichmentCD3D2.45
18Congenital dyserythropoietic anemia type iiibEnrichmentRACGAP12.45
19Immunodeficiency 19EnrichmentCD3D2.45
20Anemia, congenital dyserythropoietic, type iiib, autosomal recessiveEnrichmentRACGAP12.45
21Phakomatosis pigmentokeratoticaEnrichmentHRAS2.45
22Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.45
23Zap70-related severe combined immunodeficiencyEnrichmentZAP702.45
24Genetic steroid-resistant nephrotic syndromeEnrichmentARHGAP24, ARHGDIA2.19
25Anemia, congenital dyserythropoietic, type iiiaEnrichmentRACGAP12.15
26Costello syndromeEnrichmentHRAS2.15
27Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.15
28Spastic paraplegia 70, autosomal recessiveEnrichmentARHGAP92.15
29Trypsinogen deficiencyEnrichmentTRB2.15
30Immunodeficiency 17EnrichmentCD3G2.15
31Common variable immunodeficiency phenotype due to cd19/cd81 deficiencyEnrichmentCD192.15
32Wooly hair nevusEnrichmentHRAS2.15
33Chromosome 8p11 myeloproliferative syndromeEnrichmentBCR1.98
34Large congenital melanocytic nevusEnrichmentHRAS1.98
35SpermatocytomaEnrichmentHRAS1.98
36Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.85
37Chromosome 22q11.2 deletion syndrome, distalEnrichmentBCR1.85
38Epidermolytic nevusEnrichmentHRAS1.85
39Vitamin d-dependent rickets, type 2aEnrichmentTRB1.76
40Nevus, epidermalEnrichmentHRAS1.61
41Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.61
42Leukemia, chronic myeloidEnrichmentBCR1.61
43Noonan syndrome 3EnrichmentHRAS1.61
44Pilomyxoid astrocytomaEnrichmentSRGAP31.61
45Follicular thyroid carcinomaEnrichmentHRAS1.61
46Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.61
47Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.61
48B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentBCR1.61
49Melanocytic nevus syndrome, congenitalEnrichmentHRAS1.55
50Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.50
51Arteriovenous malformationEnrichmentHRAS1.50
52Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.46
53Combined immunodeficiencyEnrichmentZAP701.42
54Lung non-small cell carcinomaEnrichmentHRAS1.42
55Combined t cell and b cell immunodeficiencyEnrichmentZAP701.42
56Combined t and b cell immunodeficiencyEnrichmentZAP701.42
57Lip and oral cavity carcinomaEnrichmentHRAS1.38
58Hereditary chronic pancreatitisEnrichmentTRB1.31
59Noonan syndrome and noonan-related syndromeEnrichmentHRAS1.29
60RhabdomyosarcomaEnrichmentHRAS1.26
61Pancreatitis, hereditaryEnrichmentTRB1.23
62Parkinson's diseaseEnrichmentTNK21.19
63Noonan syndrome 1EnrichmentHRAS1.11
64Hydrops fetalis, nonimmuneEnrichmentHRAS1.05
65RasopathyEnrichmentHRAS1.05
66Bladder cancerEnrichmentHRAS1.01
67Differentiated thyroid carcinomaEnrichmentHRAS1.01
68Non-immune hydrops fetalisEnrichmentHRAS0.98
69Autosomal recessive non-syndromic intellectual disabilityEnrichmentEZR0.73
70Complex neurodevelopmental disorderEnrichmentTIAM10.45

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