Transport of Mature Transcript to Cytoplasm

No Pathway Network information available for Transport of Mature Transcript to Cytoplasm

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

Disorders associated with Transport of Mature Transcript to Cytoplasm SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Genetic steroid-resistant nephrotic syndromeEnrichmentNUP107, NUP133, NUP160, NUP205, NUP37, NUP85, NUP939.28
2Familial infantile bilateral striatal necrosisEnrichmentNUP54, NUP623.76
3Galloway-mowat syndromeEnrichmentNUP107, NUP1332.89
4Robin sequence with cleft mandible and limb anomaliesEnrichmentEIF4A32.26
5Intellectual developmental disorder, x-linked, syndromic 14EnrichmentUPF3B2.26
6Fetal akinesia deformation sequence 4EnrichmentNUP882.26
7Neurodevelopmental disorder with achalasia, polyneuropathy, and alacrimaEnrichmentNDC12.26
8Atrial fibrillation, familial, 15EnrichmentNUP1552.26
9Dystonia 37, early-onset, with striatal lesionsEnrichmentNUP542.26
10Nephrotic syndrome, type 19EnrichmentNUP1602.26
11Developmental delay, dysmorphic facies, and brain anomaliesEnrichmentU2AF22.26
12Galloway-mowat syndrome 8EnrichmentNUP1332.26
13Arthrogryposis multiplex congenita 7, x-linkedEnrichmentTHOC22.26
14Pontocerebellar hypoplasia, type 15EnrichmentCDC402.26
15Nephrotic syndrome, type 13EnrichmentNUP2052.26
16Microcephaly 24, primary, autosomal recessiveEnrichmentNUP372.26
17Galloway-mowat syndrome 7EnrichmentNUP1072.26
18Nephrotic syndrome, type 12EnrichmentNUP932.26
19Nephrotic syndrome, type 11EnrichmentNUP1072.26
20Encephalopathy, acute, infection-induced 9EnrichmentNUP2142.26
21Sandestig-stefanova syndromeEnrichmentNUP1882.26
22Ovarian dysgenesis 6EnrichmentNUP1072.26
23Intellectual developmental disorder, autosomal recessive 79EnrichmentTPR2.26
24Retinitis pigmentosa 84EnrichmentDHX382.26
25Nephrotic syndrome, type 18EnrichmentNUP1332.26
26Syndromic x-linked intellectual disability 14EnrichmentUPF3B2.26
27Deafness, autosomal dominant 86EnrichmentTHOC12.26
28Familial acute necrotizing encephalopathyEnrichmentRANBP22.26
29Autism 19EnrichmentEIF4E2.21
30Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizuresEnrichmentCPSF32.21
31Lethal congenital contracture syndrome 1EnrichmentGLE11.96
32Camptodactyly-arthropathy-coxa vara-pericarditis syndromeEnrichmentTPR1.96
33Striatonigral degeneration, infantileEnrichmentNUP621.96
34Intellectual developmental disorder, x-linked, syndromic, kumar typeEnrichmentTHOC21.96
35Congenital arthrogryposis with anterior horn cell diseaseEnrichmentGLE11.96
36Beaulieu-boycott-innes syndromeEnrichmentTHOC61.96
37Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalitiesEnrichmentSRSF11.96
38Nephrotic syndrome, type 17EnrichmentNUP851.96
39Immunodeficiency 127EnrichmentTHOC21.96
40Acute myeloid leukemia with t(6;9) (p23;q34.1)EnrichmentNUP2141.96
41Acute necrotizing encephalopathy of childhoodEnrichmentRANBP21.96
42Neurodevelopmental disorder with hypotonia, microcephaly, and seizuresEnrichmentCPSF31.91
43Myopia 27, autosomal dominantEnrichmentCPSF11.91
44Chronic eosinophilic leukemiaEnrichmentFIP1L11.91
45Intellectual developmental disorder, x-linked, syndromic, lujan-fryns typeEnrichmentUPF3B1.79
46Thrombocytopenia-absent radius syndromeEnrichmentRBM8A1.79
47Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentRANBP21.79
48Leukemia, acute myeloidEnrichmentNUP214, SRSF21.70
49Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessiveEnrichmentRANBP21.66
50Achalasia-addisonianism-alacrima syndromeEnrichmentAAAS1.66
51Chronic myelomonocytic leukemiaEnrichmentSRSF21.66
52Ectodermal dysplasiaEnrichmentRANBP21.66
53Systemic mastocytosis with associated hematologic neoplasmEnrichmentSRSF21.66
54Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentRANBP21.57
55Autosomal recessive hypohidrotic ectodermal dysplasia syndromeEnrichmentRANBP21.57
56Aggressive systemic mastocytosisEnrichmentSRSF21.57
57Primary hypereosinophilic syndromeEnrichmentFIP1L11.52
58Inflammatory myofibroblastic tumorEnrichmentRANBP21.49
59Mitochondrial dna depletion syndrome 4aEnrichmentRANBP21.43
60Mitochondrial dna depletion syndrome 4bEnrichmentRANBP21.37
61Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentSRSF21.32
62Myelodysplastic syndromeEnrichmentU2AF11.23
6346 xx gonadal dysgenesisEnrichmentNUP1071.20
64Seckel syndromeEnrichmentNUP851.13
65Acute promyelocytic leukemiaEnrichmentFIP1L11.12
66Pontocerebellar hypoplasiaEnrichmentCDC401.03
67LeukodystrophyEnrichmentU2AF20.98
68Focal segmental glomerulosclerosisEnrichmentNUP930.98
69Tooth agenesisEnrichmentRANBP20.95
70Precursor t-cell acute lymphoblastic leukemiaEnrichmentNUP2140.93
71Familial atrial fibrillationEnrichmentNUP1550.91
72Hirschsprung disease 1EnrichmentNUP980.83
73Differentiated thyroid carcinomaEnrichmentTPR0.83
74Primary autosomal recessive microcephalyEnrichmentNUP370.79
75Non-syndromic x-linked intellectual disabilityEnrichmentUPF3B0.75
76Fetal akinesia deformation sequence 1EnrichmentNUP880.74
77Nephrotic syndromeEnrichmentNUP930.68
78Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentGLE10.56
79Autosomal recessive non-syndromic intellectual disabilityEnrichmentTPR0.56
80Congenital nervous system abnormalityEnrichmentAAAS0.36
81Nervous system diseaseEnrichmentAAAS0.36
82MicrocephalyEnrichmentNUP1880.31
83Complex neurodevelopmental disorderEnrichmentCPSF30.27
84Retinitis pigmentosaEnrichmentDHX380.16
85Hereditary retinal dystrophyEnrichmentDHX380.10
86Fundus dystrophyEnrichmentDHX380.10

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