Transcriptional Regulation by E2F6

No Pathway Network information available for Transcriptional Regulation by E2F6

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

Disorders associated with Transcriptional Regulation by E2F6 SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Weaver syndromeEnrichmentEZH2, SUZ124.74
2Pancreatic cancerEnrichmentBRCA1, RBBP82.75
3Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.60
4Spermatogenic failure, x-linked, 9EnrichmentRBBP72.60
5Seckel syndrome 2EnrichmentRBBP82.60
6Mirror movements 2EnrichmentRAD512.60
7Microcephaly 11, primary, autosomal recessiveEnrichmentPHC12.60
8Luo-schoch-yamamoto syndromeEnrichmentRNF22.60
9Fanconi anemia, complementation group rEnrichmentRAD512.60
10Imagawa-matsumoto syndromeEnrichmentSUZ122.60
11Infant-type hemispheric gliomaEnrichmentBRCA12.60
12Jawad syndromeEnrichmentRBBP82.60
13Polydactyly-macrocephaly syndromeEnrichmentMAX2.60
14Cohen-gibson syndromeEnrichmentEED2.60
15Turnpenny-fry syndromeEnrichmentPCGF22.60
16Premature ovarian failure 26EnrichmentMGA2.60
17Oocyte/zygote/embryo maturation arrest 21EnrichmentCHEK12.60
18Primary peritoneal carcinomaEnrichmentBRCA12.60
19Fanconi anemia, complementation group aEnrichmentBRCA1, RAD512.46
20Inherited cancer-predisposing syndromeEnrichmentBRCA1, EZH2, MAX2.36
21Fanconi anemia, complementation group sEnrichmentBRCA12.30
22Pancreatic cancer 4EnrichmentBRCA12.30
23Kleefstra syndromeEnrichmentEHMT12.30
24Inflammatory breast carcinomaEnrichmentBRCA12.30
25Peritoneum cancerEnrichmentBRCA12.30
26Bilateral breast cancerEnrichmentBRCA12.30
27Kleefstra syndrome due to a point mutationEnrichmentEHMT12.30
28Hereditary breast carcinomaEnrichmentBRCA1, RAD512.27
29Spindle cell sarcomaEnrichmentMGA2.12
30Hereditary breast ovarian cancer syndromeEnrichmentBRCA1, RAD512.08
31Mirror movements 1EnrichmentRAD512.00
32Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA12.00
33CholangiocarcinomaEnrichmentBRCA12.00
34Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentCHEK12.00
35Breast-ovarian cancer, familial 2EnrichmentBRCA11.90
36Ciliary dyskinesia, primary, 40EnrichmentE2F61.90
37Endometrial stromal sarcomaEnrichmentSUZ121.90
38Kleefstra syndrome 1EnrichmentEHMT11.83
39Breast cancerEnrichmentBRCA1, RAD511.82
40PolymicrogyriaEnrichmentEHMT11.61
41Uterine corpus cancerEnrichmentBRCA11.56
42Autism spectrum disorderEnrichmentEED, EHMT11.52
43Breast-ovarian cancer, familial 1EnrichmentBRCA11.49
44PheochromocytomaEnrichmentMAX1.46
45Periventricular nodular heterotopiaEnrichmentBRCA11.46
46Seckel syndromeEnrichmentRBBP81.46
47RhabdomyosarcomaEnrichmentBRCA11.40
48Isolated congenital microcephalyEnrichmentPHC11.40
49Endometrial cancerEnrichmentBRCA11.29
50Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentMAX1.29
51Bladder cancerEnrichmentBRCA11.15
52Prostate cancerEnrichmentBRCA11.15
53Lung cancerEnrichmentBRCA11.11
54Primary autosomal recessive microcephalyEnrichmentPHC11.11
55Gastric cancerEnrichmentBRCA10.99
56Myeloma, multipleEnrichmentMGA0.88
57SchizophreniaEnrichmentEHMT10.86
58Colorectal cancerEnrichmentBRCA10.71
59Ovarian cancerEnrichmentBRCA10.65
60Complex neurodevelopmental disorderEnrichmentRNF20.57

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