Cell cycle_Role of APC in cell cycle regulation

No Pathway Network information available for Cell cycle_Role of APC in cell cycle regulation

Pathways in the Cell cycle_Role of APC in cell cycle regulation SuperPath

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

Disorders associated with Cell cycle_Role of APC in cell cycle regulation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Mosaic variegated aneuploidy syndromeEnrichmentBUB1, BUB1B, BUB35.48
2Meier-gorlin syndrome 1EnrichmentCDC6, GMNN, ORC15.15
3Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB3.26
4Deafness, autosomal recessive 32, with or without immotile spermEnrichmentCDC14A2.40
5Premature chromatid separation traitEnrichmentBUB1B2.40
6Fanconi anemia, complementation group vEnrichmentMAD2L22.40
7Oocyte/zygote/embryo maturation arrest 14EnrichmentCDC202.40
8Intellectual developmental disorder with polymicrogyria and seizuresEnrichmentTCP12.40
9Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessiveEnrichmentCCT52.40
10Cardioacrofacial dysplasia 2EnrichmentPRKACB2.40
11Ferguson-bonni neurodevelopmental syndromeEnrichmentANAPC72.40
12Developmental and epileptic encephalopathy 109EnrichmentFZR12.40
13Autosomal recessive sensory neuropathy with spastic paraplegiaEnrichmentCCT52.40
14Spondyloepimetaphyseal dysplasia with joint laxity, type 2EnrichmentKIF222.40
15Rothmund-thomson syndrome, type 1EnrichmentANAPC12.40
16Retinitis pigmentosa 67EnrichmentNEK22.40
17Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.40
18Meier-gorlin syndrome 5EnrichmentCDC62.40
19Cardioacrofacial dysplasia 1EnrichmentPRKACA2.40
20Meier-gorlin syndrome 6EnrichmentGMNN2.40
21Autosomal recessive nonsyndromic deafness 32EnrichmentCDC14A2.40
22Microcephaly 30, primary, autosomal recessiveEnrichmentBUB12.40
23Neurodevelopmental disorder with speech or visual impairment and brain hypomyelinationEnrichmentCCT32.40
24Colorectal cancerEnrichmentAURKA, BUB1, BUB1B2.30
25Bleeding disorder, platelet-type, 19EnrichmentPRKACG2.10
26Night blindness, congenital stationary, type 1hEnrichmentCDCA32.10
27Fibrolamellar carcinomaEnrichmentPRKACA2.10
28Ciliary dyskinesia, primary, 22EnrichmentRASSF11.80
29Pregnancy loss, recurrent 1EnrichmentCCNB31.80
30Mosaic variegated aneuploidy syndrome 1EnrichmentBUB1B1.70
31Nk-cell enteropathyEnrichmentAURKB1.30
32Hypertension, essentialEnrichmentCDCA31.18
33Polycystic liver diseaseEnrichmentCDC25A1.18
34Autosomal dominant polycystic liver diseaseEnrichmentCDC25A1.18
35Myocardial infarctionEnrichmentCCT71.08
36Ear malformationEnrichmentCDC14A1.04
37Fanconi anemia, complementation group aEnrichmentMAD2L20.88
38Sensorineural hearing lossEnrichmentCDC14A0.76
39Myeloma, multipleEnrichmentAURKA0.70
40Undetermined early-onset epileptic encephalopathyEnrichmentFZR10.70
41Breast cancerEnrichmentCKS1B0.59
42Rare genetic deafnessEnrichmentCDC14A0.57
43Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentCDC14A0.52
44Leber plus diseaseEnrichmentCCT20.50
45Ovarian cancerEnrichmentBUB1B0.48
46Retinitis pigmentosaEnrichmentNEK20.24
47Hereditary retinal dystrophyEnrichmentNEK20.16
48Fundus dystrophyEnrichmentNEK20.16

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