Nuclear Events (kinase and transcription factor activation)

No Pathway Network information available for Nuclear Events (kinase and transcription factor activation)

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

Disorders associated with Nuclear Events (kinase and transcription factor activation) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma of soft tissueEnrichmentATF1, CREB14.62
2Histiocytoid hemangiomaEnrichmentFOS, FOSB4.10
3Specific learning disabilityEnrichmentMAPK1, RPS6KA32.97
4Charcot-marie-tooth disease, demyelinating, type 1dEnrichmentEGR22.54
5Charcot-marie-tooth disease, dominant intermediate bEnrichmentDNM22.54
6Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.54
7Wilms tumor 6EnrichmentREST2.54
8Deafness, autosomal dominant 27EnrichmentREST2.54
9Lethal congenital contracture syndrome 5EnrichmentDNM22.54
10Craniosynostosis 3EnrichmentTCF122.54
11Fibromatosis, gingival, 5EnrichmentREST2.54
12Autosomal dominant charcot-marie-tooth disease type 2mEnrichmentDNM22.54
13Charcot-marie-tooth disease type 1dEnrichmentEGR22.54
14Hypogonadotropic hypogonadism 26 with or without anosmiaEnrichmentTCF122.54
15Coffin-lowry syndromeEnrichmentRPS6KA32.35
16Noonan syndrome 13EnrichmentMAPK12.35
17Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.35
18Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.35
19Houge-janssens syndrome 2EnrichmentPPP2R1A2.35
20Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.35
21Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.35
22Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.35
235q14.3 microdeletion syndromeEnrichmentMEF2C2.35
24Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.35
25Mef2c-related disorderEnrichmentMEF2C2.35
26Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.35
27Fibromatosis, gingival, 1EnrichmentREST2.24
28Hemangiopericytoma, malignantEnrichmentNAB22.24
29Histiocytoma, angiomatoid fibrousEnrichmentCREB12.24
30Neuropathy, congenital hypomyelinating, 1, autosomal recessiveEnrichmentEGR22.24
31Sifrim-hitz-weiss syndromeEnrichmentCHD42.24
32Menke-hennekam syndrome 2EnrichmentEP3002.24
33Myopathy, centronuclear, x-linkedEnrichmentDNM22.07
34Charcot-marie-tooth disease type 1EnrichmentEGR22.07
35Scoliosis, isolated 1EnrichmentMAPK72.05
36Houge-janssens syndrome 1EnrichmentPPP2R5D2.05
37Houge-janssens syndrome 3EnrichmentPPP2CA2.05
38Congenital generalized lipodystrophyEnrichmentFOS1.94
39Non-syndromic bicoronal craniosynostosisEnrichmentTCF121.94
40Haddad syndromeEnrichmentASCL11.94
41Gingival fibromatosisEnrichmentREST1.94
42Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.94
43Hypertrophic neuropathy of dejerine-sottasEnrichmentEGR21.84
44Chondrosarcoma, extraskeletal myxoidEnrichmentTCF121.84
45Rubinstein-taybi syndrome 2EnrichmentEP3001.84
46Myopathy, centronuclear, 1EnrichmentDNM21.77
47Rubinstein-taybi syndrome 1EnrichmentEP3001.77
48Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.77
49Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.75
50Charge syndromeEnrichmentEP3001.59
51Gastroesophageal refluxEnrichmentRPS6KA31.45
52Orthostatic intoleranceEnrichmentRPS6KA31.45
53Ventricular septal defectEnrichmentRPS6KA31.40
54Polydactyly, postaxial, type a1EnrichmentEP3001.37
55Wilms tumor 1EnrichmentREST1.37
56Rare genetic intellectual disabilityEnrichmentEP3001.37
57Charcot-marie-tooth disease type 4EnrichmentEGR21.30
58CraniosynostosisEnrichmentTCF121.25
59Centronuclear myopathyEnrichmentDNM21.23
60Heart, malformation ofEnrichmentMAPK11.11
61Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP61.11
62Autism spectrum disorderEnrichmentMEF2C, TCF121.06
63Kallmann syndromeEnrichmentDUSP61.01
64MicrocephalyEnrichmentEP300, MAPK10.98
65MyopathyEnrichmentDNM20.96
66Charcot-marie-tooth diseaseEnrichmentDNM20.95
67Lung cancerEnrichmentPPP2R1B0.87
68Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentREST0.86
69Myeloma, multipleEnrichmentSGK10.83
70Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.82
71HypertelorismEnrichmentRPS6KA30.68
72Colorectal cancerEnrichmentEP3000.65
73Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.64
74Complex neurodevelopmental disorderEnrichmentPPP2CA0.37

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