H19 action Rb-E2F1 signaling and CDK-Beta-catenin activity

No Pathway Network information available for H19 action Rb-E2F1 signaling and CDK-Beta-catenin activity

Pathways in the H19 action Rb-E2F1 signaling and CDK-Beta-catenin activity SuperPath

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

Disorders associated with H19 action Rb-E2F1 signaling and CDK-Beta-catenin activity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Colorectal cancerEnrichmentCDH1, CTNNB14.39
2Ovarian cancerEnrichmentCDH1, CTNNB14.26
3Adenoid ameloblastomaEnrichmentCTNNB13.83
4Breast lobular carcinomaEnrichmentCDH13.83
5Microcystic stromal tumorEnrichmentCTNNB13.83
6Heart, malformation ofEnrichmentCDK8, JAG13.82
7HepatoblastomaEnrichmentCTNNB1, JAG13.69
8Blepharocheilodontic syndrome 1EnrichmentCDH13.53
9Osteopathia striata with cranial sclerosisEnrichmentCTNNB13.53
10Childhood hepatocellular carcinomaEnrichmentCTNNB13.53
11Juvenile nasopharyngeal angiofibromaEnrichmentCTNNB13.53
12TeratomaEnrichmentCTNNB13.53
13Inherited cancer-predisposing syndromeEnrichmentCDH1, CDK4, RB13.52
14Bladder cancerEnrichmentCTNNB1, RB13.40
15Desmoid disease, hereditaryEnrichmentCTNNB13.35
16Neurodevelopmental disorder with spastic diplegia and visual defectsEnrichmentCTNNB13.35
17Anus, imperforateEnrichmentCTNNB13.35
18Exudative vitreoretinopathy 7EnrichmentCTNNB13.35
19Desmoid tumorEnrichmentCTNNB13.35
20Diffuse gastric and lobular breast cancer syndromeEnrichmentCDH13.23
21PilomatrixomaEnrichmentCTNNB13.23
22Alazami syndromeEnrichmentCTNNB13.23
23CraniopharyngiomaEnrichmentCTNNB13.23
24Exudative vitreoretinopathy 1EnrichmentCTNNB13.13
25Gastric cancerEnrichmentCDH1, CDK43.06
26Weyers acrofacial dysostosisEnrichmentCTNNB13.05
27Adrenocortical carcinomaEnrichmentCTNNB13.05
28Cleft lip with or without cleft palateEnrichmentCDH13.05
29Gallbladder cancerEnrichmentCTNNB12.99
30Melanoma, cutaneous malignant 3EnrichmentCDK42.99
31Intellectual developmental disorder with speech delay and dysmorphic faciesEnrichmentSOX42.99
32Charcot-marie-tooth disease, axonal, type 2hhEnrichmentJAG12.99
33Hepatorenocardiac degenerative fibrosisEnrichmentTULP32.99
34Deafness, congenital heart defects, and posterior embryotoxonEnrichmentJAG12.99
35Trilateral retinoblastomaEnrichmentRB12.99
36Lung oat cell carcinomaEnrichmentRB12.99
37Exudative vitreoretinopathyEnrichmentCTNNB12.93
38Adult hepatocellular carcinomaEnrichmentCTNNB12.88
39Ebstein anomalyEnrichmentCDK82.69
40Chromosome 13q14 deletion syndromeEnrichmentRB12.69
41Intellectual developmental disorder with hypotonia and behavioral abnormalitiesEnrichmentCDK82.69
42Brachydactyly-elbow wrist dysplasia syndromeEnrichmentMACROH2A12.69
43Familial retinoblastomaEnrichmentRB12.69
44MedulloblastomaEnrichmentCTNNB12.69
45Cleft lip/palateEnrichmentCDH12.69
46Polycystic liver diseaseEnrichmentCTNNB12.60
47Autosomal dominant polycystic liver diseaseEnrichmentCTNNB12.60
48RetinoblastomaEnrichmentRB12.51
49Alagille syndrome 1EnrichmentJAG12.51
50Osteogenic sarcomaEnrichmentRB12.51
51Woolly hair, autosomal recessive 3EnrichmentRB12.51
52Hypotrichosis 8EnrichmentRB12.51
53Dedifferentiated liposarcomaEnrichmentCDK42.51
54Squamous cell carcinomaEnrichmentRB12.51
55Bone osteosarcomaEnrichmentRB12.51
56Well-differentiated liposarcomaEnrichmentCDK42.51
57Endometrial cancerEnrichmentCDH12.51
58Hepatocellular carcinomaEnrichmentCTNNB12.49
59Small cell cancer of the lungEnrichmentRB12.38
60Lynch syndrome 4EnrichmentRB12.38
61Mantle cell lymphomaEnrichmentCCND12.38
62Middle aortic syndromeEnrichmentJAG12.38
63Prostate cancerEnrichmentCDH12.37
64Von hippel-lindau syndromeEnrichmentCCND12.29
65Hereditary breast carcinomaEnrichmentCDH12.19
66Leukemia, chronic lymphocyticEnrichmentCCND11.99
67Breast cancerEnrichmentCDH11.96
68Lip and oral cavity carcinomaEnrichmentRB11.91
69Diaphragmatic hernia, congenitalEnrichmentCDK81.87
70Lung cancer susceptibility 3EnrichmentRB11.84
71Coffin-siris syndrome 1EnrichmentSOX41.81
72Congenital nervous system abnormalityEnrichmentCTNNB11.81
73Nervous system diseaseEnrichmentCTNNB11.81
74Hydrocephalus, congenital, 1EnrichmentCDK81.79
75Melanoma, cutaneous malignant 1EnrichmentCDK41.76
76MicrocephalyEnrichmentCTNNB11.74
77Tetralogy of fallotEnrichmentJAG11.58
78Myeloma, multipleEnrichmentCCND11.25
79Complex neurodevelopmental disorderEnrichmentCDK80.92
80Hereditary retinal dystrophyEnrichmentJAG10.58
81Fundus dystrophyEnrichmentJAG10.58

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