Sumoylation by RanBP2 regulates transcriptional repression

No Pathway Network information available for Sumoylation by RanBP2 regulates transcriptional repression

Pathways in the Sumoylation by RanBP2 regulates transcriptional repression SuperPath

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

Disorders associated with Sumoylation by RanBP2 regulates transcriptional repression SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Orofacial cleft 10EnrichmentSUMO13.66
2Tooth agenesisEnrichmentRANBP2, SUMO13.58
3Nephronophthisis-like nephropathy 1EnrichmentRANGAP13.35
4Accelerated tumor formationEnrichmentMDM22.96
5Chromosome 2q37 deletion syndromeEnrichmentHDAC42.96
6Lessel-kubisch syndromeEnrichmentMDM22.96
7Encephalopathy, acute, infection-induced 9EnrichmentNUP2142.96
8Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.96
9Familial acute necrotizing encephalopathyEnrichmentRANBP22.96
10Striatonigral degeneration, infantileEnrichmentNUP622.66
11Acute myeloid leukemia with t(6;9) (p23;q34.1)EnrichmentNUP2142.66
12Primary mediastinal large b-cell lymphomaEnrichmentXPO12.66
13Acute necrotizing encephalopathy of childhoodEnrichmentRANBP22.66
14Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentRANBP22.48
15Dedifferentiated liposarcomaEnrichmentMDM22.48
16Well-differentiated liposarcomaEnrichmentMDM22.48
17Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentRANBP22.35
18Ectodermal dysplasiaEnrichmentRANBP22.35
19Familial infantile bilateral striatal necrosisEnrichmentNUP622.35
20Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentRANBP22.26
21Autosomal recessive hypohidrotic ectodermal dysplasia syndromeEnrichmentRANBP22.26
22Li-fraumeni syndromeEnrichmentMDM22.18
23Inflammatory myofibroblastic tumorEnrichmentRANBP22.18
24Mitochondrial dna depletion syndrome 4aEnrichmentRANBP22.11
25Mitochondrial dna depletion syndrome 4bEnrichmentRANBP22.05
26Precursor t-cell acute lymphoblastic leukemiaEnrichmentNUP2141.60
27NephronophthisisEnrichmentPIAS11.44
28Leukemia, acute myeloidEnrichmentNUP2141.36
29Myeloma, multipleEnrichmentHDAC41.22

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