YAP1- and WWTR1 (TAZ)-stimulated gene expression

No Pathway Network information available for YAP1- and WWTR1 (TAZ)-stimulated gene expression

Pathways in the YAP1- and WWTR1 (TAZ)-stimulated gene expression SuperPath

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

Disorders associated with YAP1- and WWTR1 (TAZ)-stimulated gene expression SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Heart diseaseEnrichmentGATA4, NKX2-5, TBX56.40
2Patent foramen ovaleEnrichmentGATA4, NKX2-5, TBX56.05
3Familial atrial fibrillationEnrichmentGATA4, NKX2-5, NPPA5.66
4Malignant epithelioid hemangioendotheliomaEnrichmentWWTR1, YAP15.16
5Atrial heart septal defectEnrichmentNKX2-5, TBX54.20
6Interatrial communicationEnrichmentNKX2-5, TBX54.20
7Heart, malformation ofEnrichmentGATA4, TBX53.76
8Tetralogy of fallotEnrichmentGATA4, NKX2-53.44
9Atrial septal defect 7 with or without atrioventricular conduction defectsEnrichmentNKX2-52.96
10Hypothyroidism, congenital, nongoitrous, 5EnrichmentNKX2-52.96
11Holt-oram syndromeEnrichmentTBX52.96
12Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual developmentEnrichmentYAP12.96
13Atrioventricular septal defect 4EnrichmentGATA42.96
14Uveal coloboma-cleft lip and palate-intellectual disabilityEnrichmentYAP12.96
15Atrial septal defect 2EnrichmentGATA42.96
16Ventricular septal defect 3EnrichmentNKX2-52.96
17Testicular anomalies with or without congenital heart diseaseEnrichmentGATA42.96
18Hypoplastic left heart syndrome 2EnrichmentNKX2-52.96
198p23.1 microdeletion syndromeEnrichmentGATA42.96
20Aortic arch interruptionEnrichmentNKX2-52.96
21Atrial heart septal defect 7EnrichmentNKX2-52.96
22Partial atrioventricular septal defect with ventricular hypoplasiaEnrichmentGATA42.96
23Sveinsson chorioretinal atrophyEnrichmentTEAD12.66
24Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactylyEnrichmentRUNX22.66
25Thumb deformityEnrichmentTBX52.66
26Kyphomelic dysplasiaEnrichmentCCN22.66
27Atrial fibrillation, familial, 6EnrichmentNPPA2.66
28Spondyloepimetaphyseal dysplasia, li-shao-li typeEnrichmentCCN22.66
29Retinitis pigmentosa 14EnrichmentTEAD32.66
3046,xy sex reversal 3EnrichmentGATA42.66
31Aortic valve disease 2EnrichmentTBX52.66
32Familial isolated congenital aspleniaEnrichmentNKX2-52.66
33Deletion 5q35EnrichmentNKX2-52.66
34Isolated atrial standstillEnrichmentNPPA2.66
35Cleidocranial dysplasia 1EnrichmentRUNX22.48
36Atrial standstill 2EnrichmentNPPA2.48
37Cleidocranial dysplasiaEnrichmentRUNX22.48
38Dilated cardiomyopathyEnrichmentNKX2-5, TBX52.46
39Hereditary progressive cardiac conduction defectEnrichmentNKX2-52.35
40Mitral valve insufficiencyEnrichmentTBX52.35
41Transposition of the great arteriesEnrichmentGATA42.35
42Pseudomyogenic hemangioendotheliomaEnrichmentWWTR12.35
43Atrioventricular septal defectEnrichmentTBX52.26
44Ventricular septal defect 1EnrichmentGATA42.26
45Congenital heart defects, multiple types, 4EnrichmentGATA42.26
46Diffuse cutaneous systemic sclerosisEnrichmentCCN22.26
47Persistent truncus arteriosusEnrichmentNKX2-52.26
48Atrial septal defect 1EnrichmentTBX52.18
49Conotruncal heart malformationsEnrichmentNKX2-52.18
50Double outlet right ventricleEnrichmentNKX2-52.18
51Limited sclerodermaEnrichmentCCN22.18
52Hypothyroidism, congenital, nongoitrous, 2EnrichmentNKX2-52.11
53Hypoplastic left heart syndromeEnrichmentNKX2-52.05
54Ventricular septal defectEnrichmentTBX52.00
55Aortic valve disease 1EnrichmentNKX2-51.85
56Microphthalmia/coloboma 12EnrichmentYAP11.85
57Aortic aneurysm, familial thoracic 1EnrichmentGATA41.81
5846,xy partial gonadal dysgenesisEnrichmentGATA41.81
59Coloboma of maculaEnrichmentYAP11.78
60Long qt syndrome 1EnrichmentTBX51.49
61Left ventricular noncompactionEnrichmentNKX2-51.42
62Nephrotic syndromeEnrichmentRUNX21.33
63Myeloma, multipleEnrichmentYAP11.22
64Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentGATA41.22
65Leber plus diseaseEnrichmentTEAD31.00
66Hereditary retinal dystrophyEnrichmentTEAD30.56
67Fundus dystrophyEnrichmentTEAD30.56

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