G-protein signaling_Rac2 regulation pathway

No Pathway Network information available for G-protein signaling_Rac2 regulation pathway

Pathways in the G-protein signaling_Rac2 regulation pathway SuperPath

#NameSourceGenes
1G-protein signaling_Rac2 regulation pathwayGeneGo (Thomson Reuters)

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

Disorders associated with G-protein signaling_Rac2 regulation pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic granulomatous diseaseEnrichmentCYBA, CYBB, NCF1, NCF29.01
2Granulomatous disease, chronic, autosomal recessive, 2EnrichmentNCF1, NCF25.05
3Granulomatous disease, chronic, x-linkedEnrichmentCYBB, NCF14.75
4Granulomatous disease, chronic, autosomal recessive, 4EnrichmentCYBA2.75
5Immunodeficiency 34EnrichmentCYBB2.75
6Deafness, autosomal recessive 24EnrichmentRDX2.75
7Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosisEnrichmentRAC22.75
8Nephrotic syndrome, type 8EnrichmentARHGDIA2.75
9Short syndromeEnrichmentPIK3R12.75
10Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.75
11Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemiaEnrichmentRAC22.75
12Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.75
13Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.75
14Neurodevelopmental disorder with language delay and seizuresEnrichmentTIAM12.75
15Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopeniaEnrichmentRAC22.75
16Congenital dyserythropoietic anemia type iiibEnrichmentRACGAP12.75
17Infantile lad-like disease due to rac2 deficiencyEnrichmentRAC22.75
18Reticular dysgenesis-like severe combined immunodeficiencyEnrichmentRAC22.75
19Anemia, congenital dyserythropoietic, type iiib, autosomal recessiveEnrichmentRACGAP12.75
20Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndromeEnrichmentRAC22.75
21Anemia, congenital dyserythropoietic, type iiiaEnrichmentRACGAP12.45
22Granulomatous disease, chronic, autosomal recessive, 1EnrichmentNCF12.45
23Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasiaEnrichmentCYBA2.28
24Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R12.28
25Chromosome 8p11 myeloproliferative syndromeEnrichmentBCR2.28
26Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.28
27Immunodeficiency 14EnrichmentPIK3R12.28
28Autoimmune polyendocrine syndrome type 1EnrichmentCYBA2.28
29Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R22.15
30Chromosome 22q11.2 deletion syndrome, distalEnrichmentBCR2.15
31Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.15
32Leukemia, chronic myeloidEnrichmentBCR1.91
33Overgrowth syndromeEnrichmentPIK3R11.91
34B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentBCR1.91
35Cardiomyopathy, familial hypertrophic, 4EnrichmentNCF11.80
36Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.76
37Williams-beuren syndromeEnrichmentNCF11.46
38MalariaEnrichmentNOS21.40
39Precursor t-cell acute lymphoblastic leukemiaEnrichmentBCR1.40
40Genetic steroid-resistant nephrotic syndromeEnrichmentARHGDIA1.23
41Non-syndromic genetic deafnessEnrichmentRDX1.21
42Nonsyndromic hearing lossEnrichmentRDX1.14
43Myeloma, multipleEnrichmentPIK3R21.02
44Autosomal recessive non-syndromic intellectual disabilityEnrichmentEZR1.01
45Rare genetic deafnessEnrichmentRDX0.88
46Colorectal cancerEnrichmentPIK3R10.84
47Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentRDX0.83
48Complex neurodevelopmental disorderEnrichmentTIAM10.70

Loading...
Loading...
Loading...