Regulation of CDH1 Gene Transcription

Pathway network for the Regulation of CDH1 Gene Transcription SuperPath

Sources:
  • Reactome

Pathways in the Regulation of CDH1 Gene Transcription SuperPath

Gene overlap in member pathways for Regulation of CDH1 Gene Transcription SuperPath

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

Disorders associated with Regulation of CDH1 Gene Transcription SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Tessadori-bicknell-van haaften neurodevelopmental syndrome 4EnrichmentH2BC12, H4C1, H4C96.51
2Tessadori-bicknell-van haaften neurodevelopmental syndrome 1EnrichmentH4C1, H4C34.33
3Tessadori-bicknell-van haaften neurodevelopmental syndrome 2EnrichmentH4C1, H4C114.33
4Bryant-li-bhoj neurodevelopmental syndrome 2EnrichmentH3-3A, H3-3B4.33
5Weaver syndromeEnrichmentEZH2, SUZ123.86
6Tessadori-bicknell-van haaften neurodevelopmental syndrome 3EnrichmentH4C1, H4C53.86
7Bladder cancerEnrichmentARID1A, RB13.62
8Non-syndromic bicoronal craniosynostosisEnrichmentTCF12, TWIST13.56
9Trilateral retinoblastomaEnrichmentRB13.09
10Non-acquired combined pituitary hormone deficiencyEnrichmentFOXA23.09
117q31 microdeletion syndromeEnrichmentFOXP23.09
12Lung oat cell carcinomaEnrichmentRB13.09
13Glioma susceptibility 1EnrichmentH3-3A, H3C12.90
14Mowat-wilson syndromeEnrichmentZEB22.79
15Chromosome 13q14 deletion syndromeEnrichmentRB12.79
16EsotropiaEnrichmentTFAP2A2.79
17Familial retinoblastomaEnrichmentRB12.79
18Lens subluxationEnrichmentTFAP2A2.79
19RetinoblastomaEnrichmentRB12.61
20Osteogenic sarcomaEnrichmentRB12.61
21Woolly hair, autosomal recessive 3EnrichmentRB12.61
22Hypotrichosis 8EnrichmentRB12.61
23Coffin-siris syndrome 2EnrichmentARID1A2.61
24Squamous cell carcinomaEnrichmentRB12.61
25Periventricular leukomalaciaEnrichmentARID1A2.61
26Bone osteosarcomaEnrichmentRB12.61
27Childhood apraxia of speechEnrichmentFOXP22.61
28Branchiooculofacial syndromeEnrichmentTFAP2A2.49
29Small cell cancer of the lungEnrichmentRB12.49
30Lynch syndrome 4EnrichmentRB12.49
31AmblyopiaEnrichmentTFAP2A2.39
32Branchiootorenal syndrome 1EnrichmentTFAP2A2.31
33Coffin-siris syndrome 1EnrichmentARID1A, SMARCA42.25
34Branchiootorenal syndromeEnrichmentTFAP2A2.25
35MegacolonEnrichmentZEB22.25
36Melanocytic nevus syndrome, congenitalEnrichmentZEB22.19
37Combined pituitary hormone deficiencyEnrichmentFOXA22.19
38Barber-say syndromeEnrichmentTWIST22.16
39Spermatogenic failure, x-linked, 9EnrichmentRBBP72.16
40Focal facial dermal dysplasia 2, brauer-setleis typeEnrichmentTWIST22.16
41Focal facial dermal dysplasia 3, setleis typeEnrichmentTWIST22.16
42Ablepharon-macrostomia syndromeEnrichmentTWIST22.16
43Noonan syndrome 13EnrichmentMAPK12.16
44Agammaglobulinemia 8b, autosomal recessiveEnrichmentTCF32.16
45Imagawa-matsumoto syndromeEnrichmentSUZ122.16
46Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalitiesEnrichmentZMYM22.16
47Agammaglobulinemia 8a, autosomal dominantEnrichmentTCF32.16
48Meacham syndromeEnrichmentWT12.16
49Craniosynostosis 3EnrichmentTCF122.16
50Cleft palate, psychomotor retardation, and distinctive facial featuresEnrichmentKDM1A2.16
51Smarca4-deficient sarcoma of thoraxEnrichmentSMARCA42.16
52Ovarian small cell carcinomaEnrichmentSMARCA42.16
53Cohen-gibson syndromeEnrichmentEED2.16
54Bryant-li-bhoj neurodevelopmental syndrome 1EnrichmentH3-3A2.16
55Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndromeEnrichmentKDM1A2.16
56Acth-independent macronodular adrenal hyperplasia 3EnrichmentKDM1A2.16
57Hypogonadotropic hypogonadism 26 with or without anosmiaEnrichmentTCF122.16
58Cat eye syndromeEnrichmentTFAP2A2.09
59EpicanthusEnrichmentTFAP2A2.01
60Septooptic dysplasiaEnrichmentARID1A2.01
61Lip and oral cavity carcinomaEnrichmentRB12.01
62Complex neurodevelopmental disorderEnrichmentH4C3, H4C5, H4C9, ZMYM21.98
63Lung cancer susceptibility 3EnrichmentRB11.95
64Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentARID1A1.89
65Robinow-sorauf syndromeEnrichmentTWIST11.86
66Denys-drash syndromeEnrichmentWT11.86
67Nephrotic syndrome, type 4EnrichmentWT11.86
68Rhabdoid tumor predisposition syndrome 2EnrichmentSMARCA41.86
69Piebald traitEnrichmentSNAI21.86
70Frasier syndromeEnrichmentWT11.86
71Sweeney-cox syndromeEnrichmentTWIST11.86
72Hypotonia, ataxia, developmental delay, and tooth enamel defect syndromeEnrichmentCTBP11.86
73Rhabdoid tumor predisposition syndromeEnrichmentSMARCA41.86
74Otosclerosis 12EnrichmentSMARCA41.86
75Coffin-siris syndrome 4EnrichmentSMARCA41.86
76B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)EnrichmentTCF31.86
77Non-syndromic sagittal craniosynostosisEnrichmentTWIST11.86
78B-lymphoblastic leukemia/lymphoma with t(17;19)EnrichmentTCF31.86
79Desmoplastic small round cell tumorEnrichmentWT11.86
80MicrophthalmiaEnrichmentTFAP2A1.75
81Inherited cancer-predisposing syndromeEnrichmentEZH2, RB1, SMARCA4, WT11.74
82Craniosynostosis 1EnrichmentTWIST11.69
83Mesothelioma, malignantEnrichmentWT11.69
84Corneal dystrophy, posterior polymorphous, 3EnrichmentZEB11.69
85Corneal dystrophy, fuchs endothelial, 6EnrichmentZEB11.69
86Intraocular pressure quantitative trait locusEnrichmentZEB11.69
87Cushing syndrome due to bilateral macronodular adrenocortical diseaseEnrichmentKDM1A1.69
88Hydrops fetalis, nonimmuneEnrichmentARID1A1.68
89Non-immune hydrops fetalisEnrichmentARID1A1.60
90Aniridia 1EnrichmentWT11.57
91Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.57
92Saethre-chotzen syndromeEnrichmentTWIST11.57
93Corneal dystrophyEnrichmentZEB11.57
94Chondrosarcoma, extraskeletal myxoidEnrichmentTCF121.47
95Leber congenital amaurosis 10EnrichmentWT11.47
96Fuchs' endothelial dystrophyEnrichmentZEB11.47
97Endometrial stromal sarcomaEnrichmentSUZ121.47
98Corneal dystrophy, posterior polymorphous, 1EnrichmentZEB11.39
99Wolf-hirschhorn syndromeEnrichmentCTBP11.39
100Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentWT11.39
101Wilms tumor 5EnrichmentWT11.39
102HypertelorismEnrichmentTFAP2A1.38
103Waardenburg syndrome, type 2eEnrichmentSNAI21.33
104NeuroblastomaEnrichmentSMARCA41.27
105Difference of sex developmentEnrichmentWT11.27
106Myeloma, multipleEnrichmentH3C1, TCF31.25
107Leukemia, acute lymphoblastic 3EnrichmentWT11.22
108Ventricular septal defectEnrichmentSMARCA41.22
109Autosomal non-syndromic agammaglobulinemiaEnrichmentTCF31.18
110Colorectal cancerEnrichmentARID1A1.17
111Atrial heart septal defectEnrichmentSMARCA41.14
11246,xy complete gonadal dysgenesisEnrichmentWT11.14
113Interatrial communicationEnrichmentSMARCA41.14
114Specific learning disabilityEnrichmentMAPK11.14
115Ovarian cancerEnrichmentRB11.10
116Congenital nervous system abnormalityEnrichmentZEB21.08
117Nervous system diseaseEnrichmentZEB21.08
118Hypercholesterolemia, familial, 1EnrichmentSMARCA41.07
11946,xy partial gonadal dysgenesisEnrichmentWT11.04
120MicrocephalyEnrichmentARID1A1.02
121Wilms tumor 1EnrichmentWT11.01
122Familial hypercholesterolemiaEnrichmentSMARCA41.01
123Kidney diseaseEnrichmentWT11.01
124Cleft palate, isolatedEnrichmentSMARCA40.96
125Heart, malformation ofEnrichmentMAPK10.93
126CraniosynostosisEnrichmentTCF120.89
127Focal segmental glomerulosclerosisEnrichmentWT10.89
128Autism spectrum disorderEnrichmentEED, TCF120.77
129CakutEnrichmentZMYM20.68
130Genetic steroid-resistant nephrotic syndromeEnrichmentWT10.68
131Cerebral palsyEnrichmentSMARCA40.63
132Primary ovarian insufficiencyEnrichmentWT10.48

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