Rab regulation of trafficking

Pathway network for the Rab regulation of trafficking SuperPath

Sources:
  • Reactome

Pathways in the Rab regulation of trafficking SuperPath

#NameSourceGenes
1Rab regulation of traffickingReactome
2RAB GEFs exchange GTP for GDP on RABsReactome
3TBC/RABGAPsReactome

Gene overlap in member pathways for Rab regulation of trafficking SuperPath

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

Disorders associated with Rab regulation of trafficking SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Warburg micro syndrome 1EnrichmentRAB18, RAB3GAP1, RAB3GAP2, TBC1D208.19
2LymphangioleiomyomatosisEnrichmentTSC1, TSC24.97
3Tuberous sclerosis 1EnrichmentTSC1, TSC24.49
4HamartomaEnrichmentTSC1, TSC24.49
5Hermansky-pudlak syndrome due to bloc-3 deficiencyEnrichmentHPS1, HPS44.36
6Focal cortical dysplasia, type iiEnrichmentTSC1, TSC24.19
7Tuberous sclerosisEnrichmentTSC1, TSC24.19
8Isolated focal cortical dysplasia type iiEnrichmentTSC1, TSC24.19
9Adult hepatocellular carcinomaEnrichmentTSC1, TSC23.42
10Martsolf syndrome 1EnrichmentRAB3GAP1, RAB3GAP23.37
11Auditory neuropathyEnrichmentRAB33A, RAB9B, TBC1D242.79
12Deafness, autosomal recessive 86EnrichmentTBC1D242.48
13Charcot-marie-tooth disease, axonal, type 2bEnrichmentRAB7A2.48
14Charcot-marie-tooth disease type 2bEnrichmentRAB7A2.48
15Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matterEnrichmentRAB11B2.48
16Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's crampEnrichmentTBC1D242.48
17Deafness, autosomal dominant 65EnrichmentTBC1D242.48
18Warburg micro syndrome 4EnrichmentTBC1D202.48
19Tbc1d24-related disordersEnrichmentTBC1D242.48
20Focal epilepsy-intellectual disability-cerebro-cerebellar malformationEnrichmentTBC1D242.48
21Progressive myoclonic epilepsy with dystoniaEnrichmentTBC1D242.48
22Isolated megalencephalyEnrichmentTBC1D72.48
23Periodic paralysisEnrichmentTBC1D242.48
24Movement diseaseEnrichmentRAB3GAP1, TBC1D242.37
25Hermansky-pudlak syndromeEnrichmentHPS1, HPS42.36
26Hermansky-pudlak syndrome 1EnrichmentHPS1, HPS42.31
27Charcot-marie-tooth disease type 4EnrichmentSBF1, SBF22.21
28Spondyloepimetaphyseal dysplasia, x-linked, with hypomyelinating leukodystrophyEnrichmentRAB33A2.18
29Charcot-marie-tooth disease, x-linked recessive, 4, with or without cerebellar ataxiaEnrichmentRAB33A2.18
30Combined oxidative phosphorylation deficiency 6EnrichmentRAB33A2.18
31Myoclonic epilepsy, familial infantileEnrichmentTBC1D242.18
32Nephrotic syndrome, type 17EnrichmentGGA32.18
33Smith-mccort dysplasiaEnrichmentRAB33B2.18
34Developmental and epileptic encephalopathy 16EnrichmentTBC1D242.18
35Amyotrophic lateral sclerosis 12 with or without frontotemporal dementiaEnrichmentOPTN2.18
36Smith-mccort dysplasia 2EnrichmentRAB33B2.18
37Amyotrophic lateral sclerosis type 12EnrichmentOPTN2.18
38Charcot-marie-tooth disease x-linked recessive 4EnrichmentRAB33A2.18
39Proteus syndromeEnrichmentAKT12.18
40Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.18
41Amyotrophic lateral sclerosis 2, juvenileEnrichmentALS22.18
42Waisman syndromeEnrichmentRAB39B2.18
43Griscelli syndrome, type 2EnrichmentRAB27A2.18
44Spastic paralysis, infantile-onset ascendingEnrichmentALS22.18
45Warburg micro syndrome 2EnrichmentRAB3GAP22.18
46Intellectual developmental disorder, autosomal recessive 13EnrichmentTRAPPC92.18
47Parkinson disease 26, autosomal dominantEnrichmentRAB322.18
48Intellectual developmental disorder, x-linked 41EnrichmentGDI12.18
49Intellectual developmental disorder, x-linked 72EnrichmentRAB39B2.18
50Deeah syndromeEnrichmentMADD2.18
51Martsolf syndrome 2EnrichmentRAB3GAP12.18
52Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.18
53Developmental and epileptic encephalopathy 49EnrichmentDENND5A2.18
54Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophyEnrichmentTRAPPC6B2.18
55Cowden syndrome 6EnrichmentAKT12.18
56Warburg micro syndrome 3EnrichmentRAB182.18
57Hermansky-pudlak syndrome 4EnrichmentHPS42.18
58Als2-related disorderEnrichmentALS22.18
59Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophyEnrichmentTRAPPC42.18
60Intellectual disability-hyperkinetic movement-truncal ataxia syndromeEnrichmentTRAPPC112.18
61Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotoniaEnrichmentMADD2.18
62Griscelli syndromeEnrichmentRAB27A2.18
63Neurodevelopmental disorder with microcephaly, short stature, and speech delayEnrichmentTRAPPC102.18
64Capillary hemangiomaEnrichmentAKT32.18
65Autosomal recessive spastic paraplegia type 69EnrichmentRAB3GAP22.18
66Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.18
67Infantile-onset ascending hereditary spastic paralysisEnrichmentALS22.18
68Intellectual disability-obesity-brain malformations-facial dysmorphism syndromeEnrichmentTRAPPC92.18
69Akt2-related familial partial lipodystrophyEnrichmentAKT22.18
70West syndromeEnrichmentTBC1D24, TSC22.03
71Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC22.00
72Glaucoma, normal tensionEnrichmentOPTN2.00
73Tuberous sclerosis 2EnrichmentTSC22.00
74Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndromeEnrichmentTBC1D242.00
75Macrocephaly/megalencephaly syndrome, autosomal recessiveEnrichmentTBC1D72.00
76Epilepsy, progressive myoclonic, 1bEnrichmentTBC1D242.00
77Deafness, x-linked 5, with peripheral neuropathyEnrichmentRAB33A2.00
78X-linked deafness 5EnrichmentRAB33A2.00
79Xanthinuria, type iiEnrichmentTSC22.00
80Combined oxidative phosphorylation deficiencyEnrichmentRAB33A2.00
81Spondyloepiphyseal dysplasia tarda, x-linkedEnrichmentTRAPPC21.88
82Primary lateral sclerosis, juvenileEnrichmentALS21.88
83Catifa syndromeEnrichmentRIC11.88
84Encephalopathy, progressive, early-onset, with episodic rhabdomyolysisEnrichmentTRAPPC2L1.88
85Senior-loken syndrome 7EnrichmentAKT31.88
86Spondyloepiphyseal dysplasia tardaEnrichmentTRAPPC21.88
87Muscular dystrophy, limb-girdle, autosomal recessive 18EnrichmentTRAPPC111.88
88Bardet-biedl syndrome 16EnrichmentAKT31.88
89Encephalopathy, progressive, early-onset, with brain atrophy and spasticityEnrichmentTRAPPC121.88
90Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomaliesEnrichmentTRAPPC41.88
91Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndromeEnrichmentTRAPPC121.88
92Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentOPTN1.78
93Glaucoma, primary open angleEnrichmentOPTN1.70
94KeratoconusEnrichmentTSC11.70
95Pelizaeus-merzbacher diseaseEnrichmentRAB9B1.70
96Spastic paraplegia 2, x-linkedEnrichmentRAB9B1.70
97Charcot-marie-tooth disease, demyelinating, type 4b3EnrichmentSBF11.70
98Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.70
99Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.70
100Charcot-marie-tooth disease type 4b3EnrichmentSBF11.70
101Congenital diarrheaEnrichmentMON1A1.70
102Pelizeaus-merzbacher spectrum disorderEnrichmentRAB9B1.70
103TyrosinemiaEnrichmentALS21.70
104Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC21.64
105Polycystic kidney disease 1EnrichmentTSC21.64
106ParkinsonismEnrichmentTBC1D241.64
107Motor neuron diseaseEnrichmentOPTN1.64
108Non-syndromic x-linked intellectual disabilityEnrichmentGDI1, RAB39B1.63
109Achalasia-addisonianism-alacrima syndromeEnrichmentTRAPPC111.58
110Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT31.58
111ChoroideremiaEnrichmentCHM1.58
112Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT31.58
113Charcot-marie-tooth disease, demyelinating, type 4b2EnrichmentSBF21.58
114Charcot-marie-tooth disease type 4b2EnrichmentSBF21.58
115Mucopolysaccharidosis ivEnrichmentTRAPPC2L1.58
116Developmental and epileptic encephalopathy 14EnrichmentTBC1D241.53
117Charcot-marie-tooth diseaseEnrichmentSBF1, SBF21.52
118Kbg syndromeEnrichmentTRAPPC2L1.48
119Mucopolysaccharidosis, type ivaEnrichmentTRAPPC2L1.48
120Muscular dystrophy, limb-girdle, autosomal recessive 23EnrichmentTRAPPC111.48
121Congenital ptosisEnrichmentRAB3GAP11.48
122Night blindnessEnrichmentCHM1.48
123HemimegalencephalyEnrichmentAKT31.48
124Multiple acyl-coa dehydrogenase deficiency, severe neonatal typeEnrichmentMADD1.48
125Endometrial stromal sarcomaEnrichmentYWHAE1.48
126Specific learning disabilityEnrichmentTBC1D241.44
127Autosomal recessive intellectual developmental disorderEnrichmentTRAPPC91.41
128Breast adenocarcinomaEnrichmentAKT11.41
129HypertrichosisEnrichmentRAB3GAP11.41
130Kidney clear cell sarcomaEnrichmentYWHAE1.41
131OligospermiaEnrichmentTBC1D251.37
132Myoclonic epilepsy of unverricht and lundborgEnrichmentTBC1D241.34
133MegacolonEnrichmentAKT31.34
134Congenital nervous system abnormalityEnrichmentTBC1D24, TSC21.32
135Nervous system diseaseEnrichmentTBC1D24, TSC21.32
136Autosomal dominant polycystic kidney diseaseEnrichmentTSC21.31
137Kidney diseaseEnrichmentTSC11.31
138Isolated congenital microcephalyEnrichmentRAB11A1.29
139Spastic paraplegia 4, autosomal dominantEnrichmentTRAPPC21.29
140CryptorchidismEnrichmentRAB3GAP11.29
141Cryptorchidism, unilateral or bilateralEnrichmentRAB3GAP11.24
142Limb-girdle muscular dystrophyEnrichmentTRAPPC111.24
143Cowden syndromeEnrichmentAKT11.24
144Juvenile amyotrophic lateral sclerosisEnrichmentALS21.24
145LeukodystrophyEnrichmentRAB33A1.19
146PolymicrogyriaEnrichmentAKT31.19
147Inherited cancer-predisposing syndromeEnrichmentTSC1, TSC21.15
148Autism spectrum disorderEnrichmentSBF1, TRAPPC9, TSC21.12
149Muscular dystrophy, limb-girdle, autosomal recessive 2EnrichmentTRAPPC111.11
150MeningiomaEnrichmentAKT11.11
151Developmental and epileptic encephalopathy 1EnrichmentTBC1D241.10
152Cleft lip/palateEnrichmentRIC11.05
153Bladder cancerEnrichmentTSC11.04
154Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentALS2, OPTN1.01
155Cleft palate, isolatedEnrichmentRAB3GAP10.97
156Esophageal atresia/tracheoesophageal fistulaEnrichmentRAB3GAP20.92
157Autosomal recessive limb-girdle muscular dystrophyEnrichmentTRAPPC110.92
158Macs syndromeEnrichmentRIN20.90
159Benign epilepsy with centrotemporal spikesEnrichmentTBC1D240.89
160Centralopathic epilepsyEnrichmentTBC1D240.88
161Multisystem inflammatory syndrome in childrenEnrichmentRAB27A0.87
162Sensorineural hearing lossEnrichmentRAB33A0.83
163Autoinflammatory diseaseEnrichmentRAB27A0.83
164Muscular dystrophyEnrichmentTRAPPC110.83
165Autosomal dominant non-syndromic intellectual disabilityEnrichmentRAB11A0.81
166Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentTBC1D240.80
167Hirschsprung disease 1EnrichmentDENND30.76
168Primary autosomal recessive microcephalyEnrichmentTRAPPC100.72
169Connective tissue diseaseEnrichmentTRAPPC20.72
170Complex neurodevelopmental disorderEnrichmentMADD, TRAPPC40.70
171Genetic steroid-resistant nephrotic syndromeEnrichmentGAPVD10.69
172Eye diseaseEnrichmentCHM0.68
173Ovarian cancerEnrichmentAKT1, TSC20.63
174Type 2 diabetes mellitusEnrichmentAKT20.61
175Bardet-biedl syndromeEnrichmentTRAPPC30.61
176Hereditary spastic paraplegiaEnrichmentRAB9B0.61
177Hereditary breast carcinomaEnrichmentAKT10.59
178Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentTBC1D240.59
179Autosomal recessive non-syndromic intellectual disabilityEnrichmentTRAPPC90.49
180SchizophreniaEnrichmentTRAPPC90.49
181Breast cancerEnrichmentAKT10.40
182Colorectal cancerEnrichmentAKT10.36
183Retinitis pigmentosaEnrichmentCHM0.12
184Hereditary retinal dystrophyEnrichmentCHM0.07
185Fundus dystrophyEnrichmentCHM0.07

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