Transcription_Transcription factor Tubby signaling pathways

No Pathway Network information available for Transcription_Transcription factor Tubby signaling pathways

Pathways in the Transcription_Transcription factor Tubby signaling pathways SuperPath

#NameSourceGenes
1Transcription_Transcription factor Tubby signaling pathwaysGeneGo (Thomson Reuters)

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

Disorders associated with Transcription_Transcription factor Tubby signaling pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma, uvealEnrichmentGNA11, GNAQ, PLCB46.90
2Phakomatosis cesioflammeaEnrichmentGNA11, GNAQ5.45
3Anastomosing haemangiomaEnrichmentGNA11, GNAQ4.98
4Capillary malformations, congenitalEnrichmentGNA11, GNAQ4.45
5Hypocalciuric hypercalcemia, familial, type iiEnrichmentGNA112.72
6Donohue syndromeEnrichmentINSR2.72
7Hyperinsulinemic hypoglycemia, familial, 5EnrichmentINSR2.72
8Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalitiesEnrichmentINSR2.72
9Diabetes mellitus, insulin-resistant, with acanthosis nigricansEnrichmentINSR2.72
10Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.72
11Sturge-weber syndromeEnrichmentGNAQ2.72
12Spondylometaphyseal dysplasia with corneal dystrophyEnrichmentPLCB32.72
13Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.72
14Auriculocondylar syndrome 2aEnrichmentPLCB42.72
15Spinocerebellar ataxia 14EnrichmentPRKCG2.72
16Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.72
17Hypocalcemia, autosomal dominant 2EnrichmentGNA112.72
18Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.72
19Congenital heart defects and ectodermal dysplasiaEnrichmentPRKD12.72
20Auriculocondylar syndrome 2bEnrichmentPLCB42.72
21Phakomatosis cesiomarmorataEnrichmentGNA112.72
22Malignant epithelial tumor of salivary glandsEnrichmentPRKD12.72
23Cutis marmorata telangiectatica congenitaEnrichmentGNA112.42
24Hyperinsulinemic hypoglycemia, familial, 4EnrichmentINSR2.42
25Maturity-onset diabetes of the young, type 10EnrichmentINS2.42
26Thrombocythemia 3EnrichmentJAK22.42
27HyperproinsulinemiaEnrichmentINS2.42
28Congenital heart defects and skeletal malformations syndromeEnrichmentABL12.42
29Autosomal dominant hypocalcemiaEnrichmentGNA112.42
30Ocular melanomaEnrichmentPLCB42.42
31Diabetes mellitus, permanent neonatal, 4EnrichmentINS2.42
32Retinal dystrophy and obesityEnrichmentTUB2.42
33PolycythemiaEnrichmentJAK22.42
34Hypereosinophilic syndromeEnrichmentJAK22.42
35Type 1 diabetes mellitus 2EnrichmentINS2.24
36Polycythemia veraEnrichmentJAK22.24
37Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentGNA112.24
38Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK22.24
39T-cell acute lymphoblastic leukemiaEnrichmentABL12.24
40Erythrocytosis, familial, 1EnrichmentJAK22.12
41Budd-chiari syndromeEnrichmentJAK22.12
42Auriculocondylar syndrome 1EnrichmentPLCB42.12
43Developmental and epileptic encephalopathy 12EnrichmentPLCB12.12
44Neonatal diabetes mellitusEnrichmentINS2.12
45Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentABL12.12
46Hereditary ataxiaEnrichmentPRKCG2.12
47Myeloproliferative neoplasmEnrichmentJAK22.02
48Klippel-trenaunay-weber syndromeEnrichmentGNAQ1.94
49Type 1 diabetes mellitusEnrichmentINS1.94
5046,xy disorder of sex developmentEnrichmentINSR1.94
51MyelofibrosisEnrichmentJAK21.87
52Leukemia, chronic myeloidEnrichmentABL11.87
53Essential thrombocythemiaEnrichmentJAK21.87
54Moyamoya angiopathyEnrichmentABL11.87
55B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentABL11.87
56Permanent neonatal diabetes mellitusEnrichmentINS1.82
57Inflammatory bowel disease 1EnrichmentPRKCQ1.77
58Leukemia, acute lymphoblastic 3EnrichmentJAK21.77
59Developmental and epileptic encephalopathy 14EnrichmentPLCB11.77
60Stroke, ischemicEnrichmentPRKCH1.72
61Diabetes mellitusEnrichmentINS1.68
62Lip and oral cavity carcinomaEnrichmentABL11.64
63Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.61
64Heart diseaseEnrichmentABL11.58
65Maturity-onset diabetes of the youngEnrichmentINS1.42
66Precursor t-cell acute lymphoblastic leukemiaEnrichmentABL11.36
67Leukemia, acute myeloidEnrichmentJAK21.13
68Benign epilepsy with centrotemporal spikesEnrichmentPLCB11.12
69Type 2 diabetes mellitusEnrichmentINSR1.11
70Centralopathic epilepsyEnrichmentPLCB11.10
71West syndromeEnrichmentPLCB11.09
72Primary ovarian insufficiencyEnrichmentJAK20.97
73MicrocephalyEnrichmentABL10.68
74Retinitis pigmentosaEnrichmentTUB0.47
75Hereditary retinal dystrophyEnrichmentTUB0.37
76Fundus dystrophyEnrichmentTUB0.37

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