Cell-type dependent selectivity of CCK2R signaling

No Pathway Network information available for Cell-type dependent selectivity of CCK2R signaling

Pathways in the Cell-type dependent selectivity of CCK2R signaling SuperPath

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

Disorders associated with Cell-type dependent selectivity of CCK2R signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hydrops fetalisEnrichmentRYR1, RYR34.52
2Arrhythmogenic right ventricular cardiomyopathyEnrichmentRYR1, RYR24.00
3Neuroocular syndrome 2, paroxysmal typeEnrichmentDAGLA3.02
4Sturge-weber syndromeEnrichmentGNAQ3.02
5Congenital myopathy 20EnrichmentRYR33.02
6Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalitiesEnrichmentGNAI13.02
7Congenital myopathy with myasthenic-like onsetEnrichmentRYR13.02
8Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathyEnrichmentRYR13.02
9Benign samaritan congenital myopathyEnrichmentRYR13.02
10Spinocerebellar ataxia 29EnrichmentITPR12.72
11Malignant hyperthermia 1EnrichmentRYR12.72
12Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndromeEnrichmentRYR22.72
13Ventricular tachycardia, catecholaminergic polymorphic, 2EnrichmentRYR22.72
14King-denborough syndromeEnrichmentRYR12.72
15Exercise-induced malignant hyperthermiaEnrichmentRYR12.72
16Phakomatosis cesioflammeaEnrichmentGNAQ2.72
17Gillespie syndromeEnrichmentITPR12.54
18Lynch syndrome 5EnrichmentRYR12.54
19Bronchopulmonary dysplasiaEnrichmentRYR12.54
20Anastomosing haemangiomaEnrichmentGNAQ2.54
21Congenital myopathy 1a, autosomal dominant, with malignant hyperthermiaEnrichmentRYR12.42
22Myopathy, centronuclear, 2EnrichmentRYR12.42
23Sacral defect with anterior meningoceleEnrichmentRYR12.42
24Amyotrophy, monomelicEnrichmentRYR32.42
25Ventricular fibrillation, paroxysmal familial, 1EnrichmentRYR22.42
26Spinocerebellar ataxia 15EnrichmentITPR12.42
27Intellectual developmental disorder, autosomal dominant 26EnrichmentRYR12.42
28Congenital myopathy 1aEnrichmentRYR12.42
29Malignant hyperthermiaEnrichmentRYR12.42
30Paroxysmal familial ventricular fibrillationEnrichmentRYR22.42
31Capillary malformations, congenitalEnrichmentGNAQ2.32
32Congenital myopathy 1b, autosomal recessiveEnrichmentRYR12.32
33Heart conduction diseaseEnrichmentRYR22.32
34Klippel-trenaunay-weber syndromeEnrichmentGNAQ2.24
35Melanoma, uvealEnrichmentGNAQ2.24
36Myopathy, centronuclear, 1EnrichmentRYR12.24
37Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentRYR22.24
38Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR12.24
39Multiple pterygium syndrome, lethal typeEnrichmentRYR12.12
40Congenital muscular dystrophyEnrichmentRYR12.12
41Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentRYR22.12
42Catecholaminergic polymorphic ventricular tachycardiaEnrichmentRYR22.12
43Autosomal dominant cerebellar ataxiaEnrichmentDAGLA2.07
44Cardiac conduction defectEnrichmentRYR21.94
45Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentRYR21.94
46Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentRYR21.94
47Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactylyEnrichmentRYR11.91
48ClubfootEnrichmentRYR11.91
49Multiple sclerosisEnrichmentITPR11.87
50Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentRYR21.87
51Congenital myopathy 4a, autosomal dominantEnrichmentRYR11.85
52Anterior segment dysgenesisEnrichmentITPR11.85
53Beckwith-wiedemann syndromeEnrichmentRYR11.77
54Neuromuscular diseaseEnrichmentRYR11.77
55Congenital myopathyEnrichmentRYR11.74
56Centronuclear myopathyEnrichmentRYR11.70
57ScoliosisEnrichmentRYR11.64
58Long qt syndromeEnrichmentRYR21.53
59Left ventricular noncompactionEnrichmentRYR21.48
60Fetal akinesia deformation sequence 1EnrichmentRYR11.46
61MyopathyEnrichmentRYR11.42
62Distal arthrogryposisEnrichmentRYR11.40
63Spastic ataxiaEnrichmentITPR11.30
64Primary ovarian insufficiencyEnrichmentRYR31.26

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