Validated nuclear estrogen receptor beta network

No Pathway Network information available for Validated nuclear estrogen receptor beta network

Pathways in the Validated nuclear estrogen receptor beta network SuperPath

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

Disorders associated with Validated nuclear estrogen receptor beta network SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Coffin-siris syndrome 1EnrichmentSMARCA4, SMARCB1, SMARCE16.31
2Rhabdoid tumor predisposition syndromeEnrichmentSMARCA4, SMARCB15.94
3Meningioma, familialEnrichmentSMARCB1, SMARCE14.20
4MeningiomaEnrichmentSMARCB1, SMARCE14.13
5Inherited cancer-predisposing syndromeEnrichmentSMARCA4, SMARCB1, SMARCE13.42
6Hemolytic uremic syndrome, atypical 5EnrichmentC32.96
7Coffin-siris syndrome 5EnrichmentSMARCE12.96
846,xy sex reversal 2EnrichmentNR0B12.96
9Adrenal hypoplasia, congenitalEnrichmentNR0B12.96
10Ovarian dysgenesis 8EnrichmentESR22.96
11Rhabdoid tumor predisposition syndrome 1EnrichmentSMARCB12.96
12NeurilemmomaEnrichmentSMARCB12.96
13Macular degeneration, age-related, 9EnrichmentC32.96
14Complement component 3 deficiency, autosomal recessiveEnrichmentC32.96
15Coffin-siris syndrome 3EnrichmentSMARCB12.96
16Smarca4-deficient sarcoma of thoraxEnrichmentSMARCA42.96
17Ovarian small cell carcinomaEnrichmentSMARCA42.96
18Complement component 3 deficiencyEnrichmentC32.96
19Facial cleftEnrichmentSMARCE12.96
20Membranoproliferative glomerulonephritisEnrichmentC32.96
21Primary membranoproliferative glomerulonephritisEnrichmentC32.96
22Rhabdoid tumor predisposition syndrome 2EnrichmentSMARCA42.66
23Schwannomatosis 1EnrichmentSMARCB12.66
24Otosclerosis 12EnrichmentSMARCA42.66
25Coffin-siris syndrome 4EnrichmentSMARCA42.66
26Thyroid carcinoma, familial medullaryEnrichmentESR22.48
27Atypical teratoid rhabdoid tumorEnrichmentSMARCB12.48
28SchwannomatosisEnrichmentSMARCB12.48
29Genetic atypical hemolytic-uremic syndromeEnrichmentC32.48
30Full schwannomatosisEnrichmentSMARCB12.35
31Nonsyndromic 46,xx testicular disorders/differences of sex developmentEnrichmentNR0B12.26
32Renal hypoplasiaEnrichmentDDX542.18
33Atypical hemolytic uremic syndrome with complement gene abnormalityEnrichmentC32.18
34NeuroblastomaEnrichmentSMARCA42.05
35Ventricular septal defectEnrichmentSMARCA42.00
36Atrial heart septal defectEnrichmentSMARCA41.92
3746,xy complete gonadal dysgenesisEnrichmentNR0B11.92
38Interatrial communicationEnrichmentSMARCA41.92
39Hypercholesterolemia, familial, 1EnrichmentSMARCA41.85
40Nk-cell enteropathyEnrichmentSMARCB11.85
4146,xy partial gonadal dysgenesisEnrichmentNR0B11.81
42Atypical hemolytic-uremic syndromeEnrichmentC31.78
43Familial hypercholesterolemiaEnrichmentSMARCA41.78
44Cleft palate, isolatedEnrichmentSMARCA41.73
45Cerebral palsyEnrichmentSMARCA41.37
46Body mass index quantitative trait locus 11EnrichmentNR0B21.27
47Ovarian cancerEnrichmentSMARCB10.97
48Autism spectrum disorderEnrichmentSMARCB10.94

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