Signaling by Hippo

No Pathway Network information available for Signaling by Hippo

Pathways in the Signaling by Hippo SuperPath

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

Disorders associated with Signaling by Hippo SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Malignant peritoneal mesotheliomaEnrichmentLATS1, LATS25.73
2Malignant epithelioid hemangioendotheliomaEnrichmentWWTR1, YAP14.95
3Deafness, autosomal dominant 51EnrichmentTJP22.85
4Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual developmentEnrichmentYAP12.85
5Memory quantitative trait locusEnrichmentWWC12.85
6Immunodeficiency 110 with lymphoproliferationEnrichmentSTK42.85
7Uveal coloboma-cleft lip and palate-intellectual disabilityEnrichmentYAP12.85
8Senior-loken syndrome 4EnrichmentNPHP42.85
9Craniofaciocardiohepatic syndromeEnrichmentAMOTL12.85
10Orofacial clefting-cardiac anomalies-facial dysmorphism syndromeEnrichmentAMOTL12.85
11Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.85
12Myeloma, multipleEnrichmentLATS1, YAP12.56
13Nephronophthisis 4EnrichmentNPHP42.55
14Cholestasis, progressive familial intrahepatic, 4EnrichmentTJP22.55
15Hypercholanemia, familial 1EnrichmentTJP22.38
16Miller-dieker lissencephaly syndromeEnrichmentYWHAE2.38
17Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE2.38
18Tethered spinal cord syndromeEnrichmentAMOTL12.38
19Acyl-coa dehydrogenase, very long-chain, deficiency ofEnrichmentDVL22.25
20Pseudomyogenic hemangioendotheliomaEnrichmentWWTR12.25
21Endometrial stromal sarcomaEnrichmentYWHAE2.16
22Branchiootorenal syndrome 1EnrichmentTJP22.08
23Familial hypercholanemiaEnrichmentTJP22.08
24Kidney clear cell sarcomaEnrichmentYWHAE2.08
25InfertilityEnrichmentNPHP42.08
26Branchiootorenal syndromeEnrichmentTJP22.01
27Primary biliary cholangitisEnrichmentTJP21.90
28Microphthalmia/coloboma 12EnrichmentYAP11.74
29Senior-loken syndrome 1EnrichmentNPHP41.74
30Cleft lip/palateEnrichmentAMOTL11.71
31Coloboma of maculaEnrichmentYAP11.68
32Kidney diseaseEnrichmentNPHP41.68
33NephronophthisisEnrichmentNPHP41.34
34Severe combined immunodeficiencyEnrichmentSTK41.34
35CakutEnrichmentNPHP41.33
36Bardet-biedl syndromeEnrichmentNPHP41.24
37Joubert syndrome 1EnrichmentNPHP41.17
38HypertelorismEnrichmentAMOTL11.15
39Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentTJP21.15
40Retinitis pigmentosaEnrichmentNPHP40.59
41Hereditary retinal dystrophyEnrichmentNPHP40.47
42Fundus dystrophyEnrichmentNPHP40.47

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