4-hydroxytamoxifen, dexamethasone, and retinoic acids regulation of p27 expression

No Pathway Network information available for 4-hydroxytamoxifen, dexamethasone, and retinoic acids regulation of p27 expression

Pathways in the 4-hydroxytamoxifen, dexamethasone, and retinoic acids regulation of p27 expression SuperPath

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

Disorders associated with 4-hydroxytamoxifen, dexamethasone, and retinoic acids regulation of p27 expression SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, MAP2K2, RAF16.13
2Noonan syndrome 1EnrichmentMAP2K1, MAP2K2, RAF15.55
3RasopathyEnrichmentMAP2K1, MAP2K2, RAF15.38
4Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K25.05
5Focal cortical dysplasia, type iiEnrichmentMTOR, TSC15.05
6Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K25.05
7Isolated focal cortical dysplasia type iiEnrichmentMTOR, TSC15.05
8Proteus syndromeEnrichmentAKT12.90
9Noonan syndrome 5EnrichmentRAF12.90
10Melorheostosis, isolatedEnrichmentMAP2K12.90
11Cardiomyopathy, dilated, 1nnEnrichmentRAF12.90
12Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.90
13Noonan syndrome 13EnrichmentMAPK12.90
14Autism 19EnrichmentEIF4E2.90
15MelorheostosisEnrichmentMAP2K12.90
16Leopard syndrome 2EnrichmentRAF12.90
17Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.90
18Cowden syndrome 6EnrichmentAKT12.90
19TrigonitisEnrichmentRAF12.90
20LymphangioleiomyomatosisEnrichmentTSC12.60
21Cebalid syndromeEnrichmentMTOR2.60
22Smith-kingsmore syndromeEnrichmentMTOR2.60
23Tafro syndromeEnrichmentMAP2K22.60
24Tuberous sclerosis 1EnrichmentTSC12.43
25Langerhans cell histiocytosisEnrichmentMAP2K12.43
26HamartomaEnrichmentTSC12.43
27Neurofibromatosis-noonan syndromeEnrichmentMAP2K22.30
28Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.30
29Tuberous sclerosisEnrichmentTSC12.30
30Noonan syndrome with multiple lentiginesEnrichmentRAF12.30
31HemimegalencephalyEnrichmentMTOR2.20
32KeratoconusEnrichmentTSC12.13
33Breast adenocarcinomaEnrichmentAKT12.13
34Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K12.06
35Renal cell carcinoma, papillary, 1EnrichmentMTOR2.06
36Noonan syndrome 3EnrichmentRAF12.06
37Pilomyxoid astrocytomaEnrichmentRAF12.06
38Overgrowth syndromeEnrichmentMTOR2.06
39Melanocytic nevus syndrome, congenitalEnrichmentRAF12.00
40Arteriovenous malformationEnrichmentMAP2K11.95
41Adult hepatocellular carcinomaEnrichmentTSC11.95
42Cowden syndromeEnrichmentAKT11.95
43Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.90
44Lung non-small cell carcinomaEnrichmentMAP2K11.86
45Specific learning disabilityEnrichmentMAPK11.86
46MeningiomaEnrichmentAKT11.83
47Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.73
48Kidney diseaseEnrichmentTSC11.73
49Rare genetic intellectual disabilityEnrichmentMTOR1.73
50Heart, malformation ofEnrichmentMAPK11.65
51Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.53
52Bladder cancerEnrichmentTSC11.45
53Familial hypertrophic cardiomyopathyEnrichmentRAF11.39
54Left ventricular noncompactionEnrichmentRAF11.37
55Hereditary breast carcinomaEnrichmentAKT11.27
56Familial isolated dilated cardiomyopathyEnrichmentRAF11.19
57Breast cancerEnrichmentAKT11.05
58Dilated cardiomyopathyEnrichmentRAF11.02
59Colorectal cancerEnrichmentAKT10.98
60Ovarian cancerEnrichmentAKT10.92
61Autism spectrum disorderEnrichmentMAP2K10.89
62MicrocephalyEnrichmentMAPK10.84
63Inherited cancer-predisposing syndromeEnrichmentTSC10.81

Loading...
Loading...
Loading...