GABA B receptor activation

Pathway network for the GABA B receptor activation SuperPath

Sources:
  • Reactome

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

Disorders associated with GABA B receptor activation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Childhood absence epilepsyEnrichmentGABRA1, GABRB3, GABRG25.79
2Undetermined early-onset epileptic encephalopathyEnrichmentGABBR2, GABRA2, GABRA5, GABRB2, GABRG25.34
3Andersen cardiodysrhythmic periodic paralysisEnrichmentKCNJ2, KCNJ55.01
4Familial atrial fibrillationEnrichmentKCNJ2, KCNJ3, KCNJ54.24
5Lennox-gastaut syndromeEnrichmentGABRB3, GABRG23.28
6Dyskinesia with orofacial involvement, autosomal dominantEnrichmentADCY53.13
7Deafness, autosomal recessive 44EnrichmentADCY13.13
8Neurodevelopmental disorder with hyperkinetic movements and dyskinesiaEnrichmentADCY53.13
9Dyskinesia with orofacial involvement, autosomal recessiveEnrichmentADCY53.13
10Dystonia 25EnrichmentGNAL3.13
11Dravet syndromeEnrichmentGABRA1, GABRG23.07
12Ventricular tachycardia, familialEnrichmentGNAI22.99
13Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalitiesEnrichmentGNAI12.99
14Lethal congenital contracture syndrome 8EnrichmentADCY62.83
15Body mass index quantitative trait locus 19EnrichmentADCY32.83
16Pituitary adenoma 4, acth-secretingEnrichmentGNAI22.69
17HypopituitarismEnrichmentGNAI22.69
18Hypomyelination neuropathy-arthrogryposis syndromeEnrichmentADCY62.66
19Chorea, benign hereditaryEnrichmentADCY52.53
20Long qt syndrome 13EnrichmentKCNJ52.50
21Short qt syndrome 3EnrichmentKCNJ22.50
22Neurodevelopmental disorder with hypotonia and dysmorphic faciesEnrichmentGNB22.50
23Hypokalemic tubulopathy and deafnessEnrichmentKCNJ162.50
24Neurodevelopmental disorder with poor language and loss of hand skillsEnrichmentGABBR22.50
25Developmental and epileptic encephalopathy 59EnrichmentGABBR22.50
26Hyperaldosteronism, familial, type iiiEnrichmentKCNJ52.50
27Seizures, sensorineural deafness, ataxia, impaired intellectual development, and electrolyte imbalanceEnrichmentKCNJ102.50
28Lodder-merla syndrome, type 2, with developmental delay and with or without cardiac arrhythmiaEnrichmentGNB52.50
29Charcot-marie-tooth disease, dominant intermediate fEnrichmentGNB42.50
30Atrial fibrillation, familial, 9EnrichmentKCNJ22.50
31Intellectual developmental disorder, autosomal dominant 42EnrichmentGNB12.50
32Sick sinus syndrome 4EnrichmentGNB22.50
33Neurodevelopmental disorder with language delay and variable cognitive abnormalitiesEnrichmentGABBR12.50
34Rare renal tubular diseaseEnrichmentKCNJ102.50
35Auriculocondylar syndrome 1EnrichmentGNAI32.38
36Achromatopsia 4EnrichmentGNAI32.38
37Developmental and epileptic encephalopathy 8EnrichmentARHGEF92.35
38Febrile seizures, familial, 8EnrichmentGABRG22.35
39Epilepsy, idiopathic generalized 13EnrichmentGABRA12.35
40Developmental and epileptic encephalopathy 74EnrichmentGABRG22.35
41Developmental and epileptic encephalopathy 79EnrichmentGABRA52.35
42Epilepsy, x-linked 2, with or without impaired intellectual development and dysmorphic featuresEnrichmentGABRA32.35
43Developmental and epileptic encephalopathy 19EnrichmentGABRA12.35
44Epilepsy, childhood absence 5EnrichmentGABRB32.35
45Developmental and epileptic encephalopathy 92EnrichmentGABRB22.35
46Developmental and epileptic encephalopathy 43EnrichmentGABRB32.35
47Developmental and epileptic encephalopathy 45EnrichmentGABRB12.35
48DystoniaEnrichmentGNAL, GNB12.26
49Keppen-lubinsky syndromeEnrichmentKCNJ62.20
50Night blindness, congenital stationary, type 1hEnrichmentGNB32.20
51Lodder-merla syndrome, type 1, with impaired intellectual development and cardiac arrhythmiaEnrichmentGNB52.20
52Cerebral visual impairmentEnrichmentGNB12.20
53Developmental and epileptic encephalopathy 78EnrichmentGABRA22.05
54Autosomal dominant non-syndromic intellectual disabilityEnrichmentGABBR1, GNB11.96
55Episodic kinesigenic dyskinesia 1EnrichmentKCNJ101.90
56Spastic paraplegia 17, autosomal dominantEnrichmentGNG31.90
57Lipodystrophy, congenital generalized, type 2EnrichmentGNG31.90
58Tobacco addictionEnrichmentGABBR21.90
59Familial sick sinus syndromeEnrichmentGNB21.90
60Thyrotoxic periodic paralysisEnrichmentGABRA31.88
61EpilepsyEnrichmentGABRA1, GABRB31.87
62Deafness, autosomal recessive 4, with enlarged vestibular aqueductEnrichmentKCNJ101.80
63Spastic diplegiaEnrichmentKCNJ101.80
64Congenital short qt syndromeEnrichmentKCNJ21.80
65Autosomal dominant nocturnal frontal lobe epilepsyEnrichmentGABRG21.76
66Pendred syndromeEnrichmentKCNJ101.72
67Rett syndromeEnrichmentGABBR21.66
68Rett syndrome, congenital variantEnrichmentGABBR21.60
69HypothyroidismEnrichmentGNB11.60
70Angelman syndromeEnrichmentGABRG31.58
71Alcohol dependenceEnrichmentGABRA21.58
72Epilepsy, childhood absence 1EnrichmentGABRB31.58
73Neurofibromatosis, type iEnrichmentGABBR11.55
74Leukemia, acute lymphoblasticEnrichmentGNB11.46
75Myelodysplastic syndromeEnrichmentGNB11.46
76Body mass index quantitative trait locus 11EnrichmentADCY31.44
77Congenital nervous system abnormalityEnrichmentGNB5, KCNJ101.35
78Nervous system diseaseEnrichmentGNB5, KCNJ101.35
79Epilepsy, myoclonic juvenileEnrichmentGABRA11.32
80Epilepsy, idiopathic generalizedEnrichmentGABRA11.32
81Hypertension, essentialEnrichmentGNB31.28
82Cleft palate, isolatedEnrichmentGNB11.28
83MicrocephalyEnrichmentGNB1, KCNJ101.24
84Generalized epilepsy with febrile seizures plusEnrichmentGABRG21.22
85Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentADCY11.20
86Attention deficit-hyperactivity disorderEnrichmentGNB51.17
87Congenital stationary night blindnessEnrichmentGNB31.15
88StrabismusEnrichmentGNB11.08
89Long qt syndrome 1EnrichmentKCNJ51.04
90Long qt syndromeEnrichmentKCNJ51.03
91Cerebral palsyEnrichmentGNB10.93
92Benign epilepsy with centrotemporal spikesEnrichmentGABRG20.78
93Centralopathic epilepsyEnrichmentGABRG20.76
94Breast cancerEnrichmentGNG30.67
95SchizophreniaEnrichmentGABRB20.64
96Autism spectrum disorderEnrichmentGNB10.53
97Complex neurodevelopmental disorderEnrichmentGNB20.49

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