RAC1 GTPase cycle

No Pathway Network information available for RAC1 GTPase cycle

Pathways in the RAC1 GTPase cycle SuperPath

#NameSourceGenes
1RAC1 GTPase cycleReactome
2CDC42 GTPase cycleReactome

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

Disorders associated with RAC1 GTPase cycle SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic granulomatous diseaseEnrichmentCYBA, CYBB, NCF1, NCF2, NCF47.27
2Wiskott-aldrich syndromeEnrichmentWAS, WIPF13.88
3Immunodeficiency 72 with autoinflammation and lymphoproliferationEnrichmentNCKAP1, NCKAP1L3.73
4Immunodeficiency 72EnrichmentNCKAP1, NCKAP1L3.73
5Adams-oliver syndrome 1EnrichmentARHGAP31, DOCK63.41
6Neural tube defectsEnrichmentDLC1, SCRIB, VANGL13.41
7Alagille syndrome 1EnrichmentFAM13A, JAG13.26
8Granulomatous disease, chronic, autosomal recessive, 2EnrichmentNCF1, NCF23.26
9Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R13.26
10Granulomatous disease, chronic, x-linkedEnrichmentCYBB, NCF12.96
11Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R22.96
12Martsolf syndrome 1EnrichmentARHGAP35, ARHGAP52.89
13Mosaic variegated aneuploidy syndrome 1EnrichmentBUB1B-PAK6, PAK62.89
14Adams-oliver syndromeEnrichmentARHGAP31, DOCK62.58
15Mosaic variegated aneuploidy syndromeEnrichmentBUB1B-PAK6, PAK62.45
16Thrombocytopenia 1EnrichmentWAS1.94
17Intellectual developmental disorder, x-linked 30EnrichmentPAK31.94
18Developmental and epileptic encephalopathy 8EnrichmentARHGEF91.94
19Autoinflammatory disease, multisystem, with immune dysregulation, x-linkedEnrichmentDOCK111.94
20Arrhythmogenic right ventricular dysplasia, familial, 12EnrichmentJUP1.94
21Lipodystrophy, congenital generalized, type 3EnrichmentCAV11.94
22Type 1 diabetes mellitus 21EnrichmentTAGAP1.94
23Cardiac valvular dysplasia 1EnrichmentPLD11.94
24Nephrotic syndrome, type 8EnrichmentARHGDIA1.94
25Charcot-marie-tooth disease, demyelinating, type 4hEnrichmentFGD41.94
26Wiskott-aldrich syndrome 2EnrichmentWIPF11.94
27Greenberg dysplasiaEnrichmentLBR1.94
28Pulmonary hypertension, primary, 3EnrichmentCAV11.94
29Pelger-huet anomalyEnrichmentLBR1.94
30Naxos diseaseEnrichmentJUP1.94
31Immunodeficiency 87 and autoimmunityEnrichmentDEF61.94
32Intellectual developmental disorder, x-linked, syndromic, billuart typeEnrichmentOPHN11.94
33Rhizomelic skeletal dysplasia with or without pelger-huet anomalyEnrichmentLBR1.94
34Knobloch syndrome 2EnrichmentPAK21.94
35Charcot-marie-tooth disease, axonal, type 2bEnrichmentRAB7A1.94
36Short syndromeEnrichmentPIK3R11.94
37Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK11.94
38Charcot-marie-tooth disease type 2bEnrichmentRAB7A1.94
39Intellectual developmental disorder, x-linked 46EnrichmentARHGEF61.94
40Lipodystrophy, familial partial, type 7EnrichmentCAV11.94
41Charcot-marie-tooth disease type 4hEnrichmentFGD41.94
42Slowed nerve conduction velocity, autosomal dominantEnrichmentARHGEF101.94
43Auditory neuropathy, autosomal dominant 1EnrichmentDIAPH31.94
44Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2EnrichmentWDR811.94
45MicrolissencephalyEnrichmentWDR811.94
46Celiac disease 4EnrichmentMYO9B1.94
47Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R11.94
48Immunodeficiency 46EnrichmentTFRC1.94
49Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R11.94
50Reynolds syndromeEnrichmentLBR1.94
51Brain small vessel disease 5 with osteoporosisEnrichmentARHGEF151.94
52Was-related disordersEnrichmentWAS1.94
53Takenouchi-kosaki syndromeEnrichmentCDC421.94
54Chilton-okur-chung neurodevelopmental syndromeEnrichmentCDC42BPB1.94
55Hydrocephalus, congenital, 3, with brain anomaliesEnrichmentWDR811.94
56Neurodevelopmental disorder with language delay and seizuresEnrichmentTIAM11.94
57Intellectual developmental disorder, autosomal dominant 63, with macrocephalyEnrichmentTRIO1.94
58Congenital dyserythropoietic anemia type iiibEnrichmentRACGAP11.94
59Nocarh syndromeEnrichmentCDC421.94
60Anemia, congenital dyserythropoietic, type iiib, autosomal recessiveEnrichmentRACGAP11.94
61MacrodactylyEnrichmentPIK3CA1.87
62Buschke-ollendorff syndromeEnrichmentLEMD31.87
63Granulomatous disease, chronic, autosomal recessive, 4EnrichmentCYBA1.87
64Amyotrophic lateral sclerosis 2, juvenileEnrichmentALS21.87
65Nance-horan syndromeEnrichmentNHS1.87
66Immunodeficiency 34EnrichmentCYBB1.87
67Noonan syndrome 4EnrichmentSOS11.87
68Spastic paralysis, infantile-onset ascendingEnrichmentALS21.87
69Megalencephaly, autosomal dominantEnrichmentPIK3CA1.87
70Cowden syndrome 5EnrichmentPIK3CA1.87
71Noonan syndrome 9EnrichmentSOS21.87
72Cerebral cavernous malformations 4EnrichmentPIK3CA1.87
73Neurodevelopmental disorder with absent language and variable seizuresEnrichmentWASF11.87
74Charcot-marie-tooth disease, axonal, type 2hhEnrichmentJAG11.87
75Retinitis pigmentosa 78EnrichmentARHGEF181.87
76Hemifacial myohyperplasiaEnrichmentPIK3CA1.87
77Immunodeficiency 40EnrichmentDOCK21.87
78Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA1.87
79Als2-related disorderEnrichmentALS21.87
80Deafness, congenital heart defects, and posterior embryotoxonEnrichmentJAG11.87
81Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxiaEnrichmentDOCK31.87
82Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA1.87
83Melorheostosis with osteopoikilosisEnrichmentLEMD31.87
84HypospadiasEnrichmentPIK3CA1.87
85Rare venous malformationEnrichmentPIK3CA1.87
86Diaphragmatic eventrationEnrichmentPIK3CA1.87
87Pik3ca-related overgrowth spectrumEnrichmentPIK3CA1.87
88Rare combined vascular malformationEnrichmentPIK3CA1.87
89Cavernous lymphangiomaEnrichmentPIK3CA1.87
90Pik3ca-related overgrowth syndromeEnrichmentPIK3CA1.87
91Isolated osteopoikilosisEnrichmentLEMD31.87
92Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC11.87
93Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA1.87
94Eccrine angiomatous hamartomaEnrichmentPIK3CA1.87
95Autosomal dominant combined immunodeficiency due to erbin deficiencyEnrichmentERBIN1.87
96Macrodactyly of toeEnrichmentPIK3CA1.87
97Infantile-onset ascending hereditary spastic paralysisEnrichmentALS21.87
98Temporomandibular joint anomalyEnrichmentDOCK11.87
99Cataract 44EnrichmentEPHA2, NHS1.66
100Anemia, congenital dyserythropoietic, type iiiaEnrichmentRACGAP11.64
101Neutropenia, severe congenital, x-linkedEnrichmentWAS1.64
102Deafness, autosomal recessive 28EnrichmentTRIO1.64
103Anemia, hypochromic microcytic, with iron overload 2EnrichmentSTEAP31.64
104Duane retraction syndrome 2EnrichmentCHN11.64
105Adams-oliver syndrome 2EnrichmentDOCK61.64
106Spastic paraplegia 70, autosomal recessiveEnrichmentARHGAP91.64
107Hypobetalipoproteinemia, familial, 2EnrichmentDOCK71.64
108Developmental and epileptic encephalopathy 23EnrichmentDOCK71.64
109Immune system diseaseEnrichmentCDC421.64
110Paget's disease of boneEnrichmentDOCK61.64
111Aarskog syndromeEnrichmentFGD11.64
112Cataract 48EnrichmentDNMBP1.64
113Crohn's diseaseEnrichmentFMNL21.64
114Malignant peripheral nerve sheath tumor with perineurial differentiationEnrichmentSH3PXD2A1.64
115Malignant triton tumorEnrichmentSH3PXD2A1.64
116Early-onset nuclear cataractEnrichmentEPHA2, NHS1.61
117Fibromatosis, gingival, 1EnrichmentSOS11.57
118Granulomatous disease, chronic, autosomal recessive, 1EnrichmentNCF11.57
119Cataract 40EnrichmentNHS1.57
120Myopathy, x-linked, with postural muscle atrophyEnrichmentEMD1.57
121Pulmonic stenosisEnrichmentSOS11.57
122Keratosis, seborrheicEnrichmentPIK3CA1.57
123Granulomatous disease, chronic, autosomal recessive, 3EnrichmentNCF41.57
124Primary lateral sclerosis, juvenileEnrichmentALS21.57
125Noonan syndrome 8EnrichmentPIK3CA1.57
126Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.57
127Rosette-forming glioneuronal tumorEnrichmentPIK3CA1.57
128Syndromic x-linked intellectual disabilityEnrichmentNHS1.57
129OsteopoikilosisEnrichmentLEMD31.57
13012q14 microdeletion syndromeEnrichmentLEMD31.57
131X-linked emery-dreifuss muscular dystrophyEnrichmentEMD1.57
132Arteriovenous malformations of the brainEnrichmentLEMD3, PREX21.57
133Hyper-ige syndrome 2, autosomal recessive, with recurrent infectionsEnrichmentDOCK81.47
134Aarskog-scott syndromeEnrichmentFGD11.47
135Intellectual developmental disorder, x-linked, syndromic, claes-jensen typeEnrichmentFGD11.47
136Spinocerebellar ataxia 4EnrichmentPLEKHG41.47
137Hypercholanemia, familial 1EnrichmentDOCK61.47
138Epidermolysis bullosa, lethal acantholyticEnrichmentJUP1.47
139Chromosome 8p11 myeloproliferative syndromeEnrichmentBCR1.47
140Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R11.47
141Hyper-ige syndrome 3, autosomal recessive, with recurrent infectionsEnrichmentDOCK81.47
142Intellectual developmental disorder, autosomal dominant 44, with microcephalyEnrichmentTRIO1.47
143Leukodystrophy and acquired microcephaly with or without dystoniaEnrichmentPLEKHG21.47
144Immunodeficiency 14EnrichmentPIK3R11.47
145Duane retraction syndromeEnrichmentCHN11.47
146Syndromic x-linked intellectual disability claes-jensen typeEnrichmentFGD11.47
147Noonan syndrome 1EnrichmentSOS1, SOS21.41
148Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasiaEnrichmentCYBA1.39
149Pompe disease, infantile-onsetEnrichmentPIK3CA1.39
150Nuchal bleb, familialEnrichmentSOS11.39
151Polycystic kidney disease 2 with or without polycystic liver diseaseEnrichmentFAM13A1.39
152Developmental and epileptic encephalopathy 65EnrichmentCYFIP21.39
153Polycystic kidney disease 2EnrichmentFAM13A1.39
154Squamous cell carcinomaEnrichmentFAM13A1.39
155Microcephaly 17, primary, autosomal recessiveEnrichmentCIT1.39
156Autoimmune polyendocrine syndrome type 1EnrichmentCYBA1.39
157KeratoacanthomaEnrichmentPIK3CA1.39
158TyrosinemiaEnrichmentALS21.39
159Intellectual developmental disorder, autosomal dominant 1EnrichmentITSN11.34
160Sacral defect with anterior meningoceleEnrichmentVANGL11.34
161Chromosome 22q11.2 deletion syndrome, distalEnrichmentBCR1.34
162Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.34
163Imerslund-grasbeck syndrome 2EnrichmentCDC42BPB1.34
164Fetal akinesia deformation sequence 3EnrichmentDOCK71.34
165Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC421.34
166OligohydramniosEnrichmentOPHN11.34
167Knobloch syndromeEnrichmentPAK21.34
168RasopathyEnrichmentSOS1, SOS21.31
169Emery-dreifuss muscular dystrophy 1, x-linkedEnrichmentEMD1.27
170Emery-dreifuss muscular dystrophyEnrichmentEMD1.27
171Cerebrovascular diseaseEnrichmentPIK3CA1.27
172Familial cerebral cavernous malformationsEnrichmentPIK3CA1.27
173Middle aortic syndromeEnrichmentJAG11.27
174Gingival fibromatosisEnrichmentSOS11.27
175Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.27
176Moebius syndromeEnrichmentCHN11.25
177Knobloch syndrome 1EnrichmentPAK21.25
178Robinow syndrome, autosomal dominant 2EnrichmentCHN11.25
179Diffuse cutaneous systemic sclerosisEnrichmentCAV11.25
180Genetic steroid-resistant nephrotic syndromeEnrichmentARHGAP24, ARHGDIA1.24
181Cataract 6, multiple typesEnrichmentEPHA21.18
182Capillary malformations, congenitalEnrichmentPIK3CA1.18
183HemimegalencephalyEnrichmentPIK3CA1.18
184AniridiaEnrichmentEPHA21.18
185Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1EnrichmentWDR811.17
186Anterior segment dysgenesis 5EnrichmentARHGAP351.17
187Megaloblastic anemiaEnrichmentCDC42BPB1.17
188Limited sclerodermaEnrichmentCAV11.17
189Thyroid cancer, nonmedullary, 2EnrichmentSRGAP11.11
190Imerslund-grasbeck syndrome 1EnrichmentCDC42BPB1.11
191Leukemia, chronic myeloidEnrichmentBCR1.11
192Pilomyxoid astrocytomaEnrichmentSRGAP31.11
193Follicular thyroid carcinomaEnrichmentSRGAP11.11
194Overgrowth syndromeEnrichmentPIK3R11.11
195Moyamoya angiopathyEnrichmentARHGEF251.11
196B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentBCR1.11
197Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.10
198Cowden syndrome 1EnrichmentPIK3CA1.10
199Hemihyperplasia, isolatedEnrichmentPIK3CA1.10
200Breast adenocarcinomaEnrichmentPIK3CA1.10
201Lung squamous cell carcinomaEnrichmentPIK3CA1.10
202Spondylocostal dysostosis 1, autosomal recessiveEnrichmentPLEKHG21.05
203Complex neurodevelopmental disorderEnrichmentDOCK3, PAK3, TIAM1, WASF11.05
204Nevus, epidermalEnrichmentPIK3CA1.04
205Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.04
206Noonan syndrome 3EnrichmentSOS11.04
207Gallbladder cancerEnrichmentPIK3CA1.04
208Inflammatory bowel disease 1EnrichmentFMNL21.00
209Early-onset posterior polar cataractEnrichmentEPHA20.98
210Peters-plus syndromeEnrichmentARHGAP350.96
211Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R10.96
212Autosomal dominant non-syndromic intellectual disabilityEnrichmentDOCK8, ITSN10.95
213Colorectal cancerEnrichmentDLC1, PIK3CA, PIK3R10.94
214Cardiomyopathy, familial hypertrophic, 4EnrichmentNCF10.93
215Coronary heart disease 5EnrichmentKALRN0.93
216Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC10.93
217Arteriovenous malformationEnrichmentPIK3CA0.93
218Adult hepatocellular carcinomaEnrichmentPIK3CA0.93
219Cowden syndromeEnrichmentPIK3CA0.93
220Juvenile amyotrophic lateral sclerosisEnrichmentALS20.93
221Combined immunodeficiencyEnrichmentTFRC0.92
222Combined t cell and b cell immunodeficiencyEnrichmentTFRC0.92
223Heritable pulmonary arterial hypertensionEnrichmentCAV10.92
224Combined t and b cell immunodeficiencyEnrichmentTFRC0.92
225Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA0.89
226Juvenile myelomonocytic leukemiaEnrichmentARHGAP260.89
227Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentJUP0.89
228Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentJUP0.89
229Hypercholesterolemia, familial, 1EnrichmentDOCK60.85
230Lung non-small cell carcinomaEnrichmentPIK3CA0.85
231Cleft lip/palateEnrichmentARHGAP290.83
232Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentJUP0.83
233MeningiomaEnrichmentPIK3CA0.82
234Lip and oral cavity carcinomaEnrichmentPIK3CA0.82
235Familial hypercholesterolemiaEnrichmentDOCK60.80
236Aortic valve disease 1EnrichmentSOS10.79
237MicrocephalyEnrichmentPAK3, TRIO, WDR810.77
238Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentKCTD30.77
239Wolff-parkinson-white syndromeEnrichmentJUP0.77
240Arrhythmogenic right ventricular cardiomyopathyEnrichmentJUP0.77
241CataractEnrichmentEPHA20.76
24246,xy partial gonadal dysgenesisEnrichmentSOS10.76
243Syndromic intellectual disabilityEnrichmentTRIO0.75
244Lynch syndromeEnrichmentPIK3CA0.73
245Noonan syndrome and noonan-related syndromeEnrichmentSOS10.73
246Charcot-marie-tooth disease type 4EnrichmentFGD40.73
247Esophageal atresia/tracheoesophageal fistulaEnrichmentITSN10.70
248Interstitial lung disease 2EnrichmentFAM13A0.68
249Heart, malformation ofEnrichmentJAG10.66
250Neuromuscular diseaseEnrichmentEMD0.66
251Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentEMD0.64
252Precursor t-cell acute lymphoblastic leukemiaEnrichmentBCR0.63
253Williams-beuren syndromeEnrichmentNCF10.62
254Endometrial cancerEnrichmentPIK3CA0.60
255HepatoblastomaEnrichmentJAG10.60
256Jeune thoracic dystrophyEnrichmentLBR0.60
257Hepatocellular carcinomaEnrichmentPIK3CA0.58
258Asphyxiating thoracic dystrophyEnrichmentLBR0.56
259Severe covid-19EnrichmentDOCK80.54
260Tetralogy of fallotEnrichmentJAG10.52
261Short-rib thoracic dysplasia 1 with or without polydactylyEnrichmentLBR0.50
262Severe combined immunodeficiencyEnrichmentDOCK80.50
263CakutEnrichmentSRGAP10.49
264Bladder cancerEnrichmentPIK3CA0.48
265Prostate cancerEnrichmentPIK3CA0.48
266Non-syndromic x-linked intellectual disabilityEnrichmentARHGEF60.47
267Developmental and epileptic encephalopathyEnrichmentARHGEF150.47
268Lung cancerEnrichmentPIK3CA0.45
269Primary autosomal recessive microcephalyEnrichmentCIT0.45
270Cerebral palsyEnrichmentARHGAP310.44
271Charcot-marie-tooth diseaseEnrichmentARHGEF100.42
272MyopathyEnrichmentEMD0.37
273ThrombocytopeniaEnrichmentWAS0.37
274Gastric cancerEnrichmentPIK3CA0.35
275Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentDIAPH30.34
276Hereditary breast carcinomaEnrichmentPIK3CA0.34
277Familial isolated dilated cardiomyopathyEnrichmentTMPO0.34
278Myeloma, multipleEnrichmentPIK3R20.32
279HypertelorismEnrichmentPIK3CA0.29
280Undetermined early-onset epileptic encephalopathyEnrichmentCYFIP20.27
281Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentALS20.26
282Dilated cardiomyopathyEnrichmentJUP0.22
283AutismEnrichmentDOCK40.20
284Breast cancerEnrichmentPIK3CA0.19
285Congenital nervous system abnormalityEnrichmentOPHN10.15
286Nervous system diseaseEnrichmentOPHN10.15
287Autism spectrum disorderEnrichmentCDC42BPB0.14
288Ovarian cancerEnrichmentPIK3CA0.12
289Hereditary retinal dystrophyEnrichmentARHGEF18, JAG10.04
290Fundus dystrophyEnrichmentARHGEF18, JAG10.04
291Retinitis pigmentosaEnrichmentARHGEF180.02

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