HSF1-dependent transactivation

Pathway network for the HSF1-dependent transactivation SuperPath

Sources:
  • Reactome

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

Disorders associated with HSF1-dependent transactivation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1InfluenzaDirect
2Rare genetic intellectual disabilityEnrichmentCREBBP, EP300, MTOR5.66
3Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3004.83
4Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3004.83
5Menke-hennekam syndrome 1EnrichmentCREBBP2.99
6Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.99
7Menke-hennekam syndromeEnrichmentCREBBP2.99
8Cardiomyopathy, dilated, 1iiEnrichmentCRYAB2.75
9Intellectual developmental disorder, autosomal recessive 63EnrichmentCAMK2A2.75
10Intellectual developmental disorder, autosomal dominant 54EnrichmentCAMK2B2.75
11Myopathy, myofibrillar, 2b, infantile-onsetEnrichmentCRYAB2.75
12Charcot-marie-tooth disease, axonal, type 2lEnrichmentHSPB82.75
13Myopathy, myofibrillar, 2a, adult-onsetEnrichmentCRYAB2.75
14Myopathy, myofibrillar, 13, with rimmed vacuolesEnrichmentHSPB82.75
15Intellectual developmental disorder, autosomal dominant 53EnrichmentCAMK2A2.75
16Intellectual developmental disorder, autosomal dominant 59EnrichmentCAMK2G2.75
17Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndromeEnrichmentHSPB82.75
18Thumb deformityEnrichmentCREBBP2.69
19Menke-hennekam syndrome 2EnrichmentEP3002.69
20Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.69
21Fibrolamellar carcinomaEnrichmentDNAJB12.69
22Tethered spinal cord syndromeEnrichmentCREBBP2.51
23Intraocular pressure quantitative trait locusEnrichmentCREBBP2.51
24Autosomal dominant non-syndromic intellectual disabilityEnrichmentCAMK2A, CAMK2B2.46
25Cardiomyopathy, familial restrictive, 1EnrichmentCRYAB2.45
26Cebalid syndromeEnrichmentMTOR2.45
27Cataract 16, multiple typesEnrichmentCRYAB2.45
28Smith-kingsmore syndromeEnrichmentMTOR2.45
29Rubinstein-taybi syndrome 2EnrichmentEP3002.29
30Distal myopathyEnrichmentHSPB82.28
31HypertrichosisEnrichmentCREBBP2.21
32Focal cortical dysplasia, type iiEnrichmentMTOR2.15
33Myopathy, autophagic vacuolar, infantile-onsetEnrichmentHSPB82.15
34Isolated focal cortical dysplasia type iiEnrichmentMTOR2.15
35AutismEnrichmentCAMK2G, CREBBP2.15
36Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB82.05
37HemimegalencephalyEnrichmentMTOR2.05
38Charge syndromeEnrichmentEP3002.03
39Renal cell carcinoma, papillary, 1EnrichmentMTOR1.91
40Overgrowth syndromeEnrichmentMTOR1.91
41Early-onset posterior polar cataractEnrichmentCRYAB1.85
42Heart diseaseEnrichmentCREBBP1.84
43Congenital nervous system abnormalityEnrichmentCAMK2B, CREBBP1.83
44Nervous system diseaseEnrichmentCAMK2B, CREBBP1.83
45Polydactyly, postaxial, type a1EnrichmentEP3001.81
46Corpus callosum, agenesis ofEnrichmentCREBBP1.81
47Isolated corpus callosum agenesisEnrichmentCREBBP1.81
48Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.81
49Early-onset lamellar cataractEnrichmentCRYAB1.71
50Diffuse large b-cell lymphomaEnrichmentCREBBP1.71
51MicrocephalyEnrichmentCAMK2B, EP3001.70
52ScoliosisEnrichmentCREBBP1.61
53Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.58
54Early-onset nuclear cataractEnrichmentCRYAB1.50
55Myeloma, multipleEnrichmentCREBBP1.25
56DystoniaEnrichmentCAMK2B1.22
57Colorectal cancerEnrichmentEP3001.06
58Familial isolated dilated cardiomyopathyEnrichmentCRYAB1.05

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