G-protein beta:gamma signalling

Pathway network for the G-protein beta:gamma signalling SuperPath

Sources:
  • Reactome

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

Disorders associated with G-protein beta:gamma signalling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neurodevelopmental disorder with hypotonia and dysmorphic faciesEnrichmentGNB22.88
2Isolated growth hormone deficiency type iiiEnrichmentBTK2.88
3Lodder-merla syndrome, type 2, with developmental delay and with or without cardiac arrhythmiaEnrichmentGNB52.88
4Charcot-marie-tooth disease, dominant intermediate fEnrichmentGNB42.88
5Intellectual developmental disorder, autosomal dominant 42EnrichmentGNB12.88
6Sick sinus syndrome 4EnrichmentGNB22.88
7Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.83
8Intellectual developmental disorder, x-linked 46EnrichmentARHGEF62.83
9Takenouchi-kosaki syndromeEnrichmentCDC422.83
10Nocarh syndromeEnrichmentCDC422.83
11Proteus syndromeEnrichmentAKT12.73
12Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.73
13Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.73
14Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.73
15Cowden syndrome 6EnrichmentAKT12.73
16Immunodeficiency 97 with autoinflammationEnrichmentPIK3CG2.73
17Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.73
18Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.73
19Capillary hemangiomaEnrichmentAKT32.73
20Akt2-related familial partial lipodystrophyEnrichmentAKT22.73
21Spondylometaphyseal dysplasia with corneal dystrophyEnrichmentPLCB32.63
22Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK2.58
23Night blindness, congenital stationary, type 1hEnrichmentGNB32.58
24Agammaglobulinemia, x-linkedEnrichmentBTK2.58
25Lodder-merla syndrome, type 1, with impaired intellectual development and cardiac arrhythmiaEnrichmentGNB52.58
26Cerebral visual impairmentEnrichmentGNB12.58
27Immune system diseaseEnrichmentCDC422.53
28Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R52.43
29Senior-loken syndrome 7EnrichmentAKT32.43
30Bardet-biedl syndrome 16EnrichmentAKT32.43
31Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK2.40
32Agammaglobulinemia 1EnrichmentBTK2.40
33Spastic paraplegia 17, autosomal dominantEnrichmentGNG32.28
34Lipodystrophy, congenital generalized, type 2EnrichmentGNG32.28
35Familial sick sinus syndromeEnrichmentGNB22.28
36Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC422.23
37Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT32.13
38Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT32.13
39Breast cancerEnrichmentAKT1, GNG32.08
40HemimegalencephalyEnrichmentAKT32.04
41Developmental and epileptic encephalopathy 12EnrichmentPLCB12.03
42HypothyroidismEnrichmentGNB11.98
43Hemihyperplasia, isolatedEnrichmentRHOA1.96
44Breast adenocarcinomaEnrichmentAKT11.96
45MegacolonEnrichmentAKT31.89
46Leukemia, acute lymphoblasticEnrichmentGNB11.84
47Myelodysplastic syndromeEnrichmentGNB11.84
48Cowden syndromeEnrichmentAKT11.78
49PolymicrogyriaEnrichmentAKT31.74
50Developmental and epileptic encephalopathy 14EnrichmentPLCB11.68
51MeningiomaEnrichmentAKT11.66
52Hypertension, essentialEnrichmentGNB31.65
53Cleft palate, isolatedEnrichmentGNB11.65
54Diffuse large b-cell lymphomaEnrichmentBTK1.60
55Attention deficit-hyperactivity disorderEnrichmentGNB51.54
56Congenital stationary night blindnessEnrichmentGNB31.52
57StrabismusEnrichmentGNB11.45
58DystoniaEnrichmentGNB11.34
59Cerebral palsyEnrichmentGNB11.30
60Non-syndromic x-linked intellectual disabilityEnrichmentARHGEF61.29
61Autosomal dominant non-syndromic intellectual disabilityEnrichmentGNB11.19
62Type 2 diabetes mellitusEnrichmentAKT21.13
63Hereditary breast carcinomaEnrichmentAKT11.11
64Benign epilepsy with centrotemporal spikesEnrichmentPLCB11.03
65Centralopathic epilepsyEnrichmentPLCB11.01
66West syndromeEnrichmentPLCB11.01
67Congenital nervous system abnormalityEnrichmentGNB50.88
68Nervous system diseaseEnrichmentGNB50.88
69Autism spectrum disorderEnrichmentGNB10.87
70Colorectal cancerEnrichmentAKT10.83
71MicrocephalyEnrichmentGNB10.82
72Complex neurodevelopmental disorderEnrichmentGNB20.82
73Ovarian cancerEnrichmentAKT10.77

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