Deadenylation-dependent mRNA decay

Pathway network for the Deadenylation-dependent mRNA decay SuperPath

Sources:
  • Reactome

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

Disorders associated with Deadenylation-dependent mRNA decay SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pontocerebellar hypoplasia, type 1eEnrichmentEXOSC3, EXOSC8, EXOSC97.57
2Trichohepatoenteric syndromeEnrichmentSKIC2, SKIC35.41
3Trichohepatoenteric syndrome 1EnrichmentSKIC2, SKIC35.11
4Complex neurodevelopmental disorderEnrichmentAGO2, CNOT1, CNOT3, EIF4A24.14
5Pontocerebellar hypoplasiaEnrichmentEXOSC3, EXOSC93.70
6Leukodystrophy and cerebellar atrophyEnrichmentLSM72.96
7Intellectual developmental disorder with impaired language and dysmorphic faciesEnrichmentDDX62.96
8Intellectual developmental disorder, autosomal recessive 50EnrichmentEDC32.96
9Ficus syndromeEnrichmentLSM12.96
10Pontocerebellar hypoplasia, type 1fEnrichmentEXOSC12.93
11Cerebellar ataxia, brain abnormalities, and cardiac conduction defectsEnrichmentEXOSC52.93
12Pontocerebellar hypoplasia, type 1cEnrichmentEXOSC82.93
13Pontocerebellar hypoplasia, type 1dEnrichmentEXOSC92.93
14Short stature, hearing loss, retinitis pigmentosa, and distinctive faciesEnrichmentEXOSC22.93
15Robin sequence with cleft mandible and limb anomaliesEnrichmentEIF4A32.73
16Rhabdomyosarcoma, embryonal, 2EnrichmentDICER12.73
17Parkinson disease 18, autosomal dominantEnrichmentEIF4G12.73
18Holoprosencephaly 12 with or without pancreatic agenesisEnrichmentCNOT12.73
19Oocyte/zygote/embryo maturation arrest 13EnrichmentZFP36L22.73
20Autism 19EnrichmentEIF4E2.73
21Dicer1 syndromeEnrichmentDICER12.73
22Pleuropulmonary blastomaEnrichmentDICER12.73
23Global developmental delay, lung cysts, overgrowth, and wilms tumorEnrichmentDICER12.73
24Neurodevelopmental disorder with hypotonia and speech delay, with or without seizuresEnrichmentEIF4A22.73
25Vissers-bodmer syndromeEnrichmentCNOT12.73
26Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomaliesEnrichmentCNOT22.73
27Oocyte/zygote/embryo maturation arrest 8EnrichmentBTG42.73
28Malignant sertoli-leydig cell tumor of ovaryEnrichmentDICER12.73
29Supratentorial primitive neuroectodermal tumorEnrichmentDICER12.73
30GynandroblastomaEnrichmentDICER12.73
31Dicer1 tumor predispositionEnrichmentDICER12.73
32Female infertility due to an implantation defect of genetic originEnrichmentZFP36L22.73
33Pancreatic agenesis-holoprosencephaly syndromeEnrichmentCNOT12.73
34Dyskeratosis congenita, autosomal recessive 6EnrichmentPARN2.73
35Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 4EnrichmentPARN2.73
36Trichohepatoenteric syndrome 2EnrichmentSKIC22.63
37Immunodeficiency 57 with autoinflammationEnrichmentSKIC22.63
38Congenital pontocerebellar hypoplasia type 1EnrichmentEXOSC32.63
39Pontocerebellar hypoplasia, type 1bEnrichmentEXOSC32.45
40Cerebellar diseaseEnrichmentEXOSC32.45
41Al-raqad syndromeEnrichmentDCPS2.45
42Premature ovarian failure 3EnrichmentAGO22.43
43Goiter, multinodular 1, with or without sertoli-leydig cell tumorsEnrichmentDICER12.43
44Vertebral anomalies and variable endocrine and t-cell dysfunctionEnrichmentDICER12.43
45Alopecia-intellectual disability syndrome 4EnrichmentCNOT12.43
46PineoblastomaEnrichmentDICER12.43
47Malignant granulosa cell tumor of the ovaryEnrichmentDICER12.43
48Lessel-kreienkamp syndromeEnrichmentAGO22.26
49Intellectual developmental disorder with speech delay, autism, and dysmorphic faciesEnrichmentCNOT32.13
50Embryonal rhabdomyosarcomaEnrichmentDICER12.13
51Histiocytoid hemangiomaEnrichmentZFP36L22.04
52Pulmonary fibrosisEnrichmentPARN1.96
53Hoyeraal-hreidarsson syndromeEnrichmentPARN1.96
54LeukodystrophyEnrichmentLSM71.66
55Congenital myopathyEnrichmentEXOSC31.65
56Autosomal recessive non-syndromic intellectual disabilityEnrichmentDCPS, EDC31.62
57LissencephalyEnrichmentEXOSC31.61
58RhabdomyosarcomaEnrichmentDICER11.54
59Interstitial lung disease 2EnrichmentPARN1.51
60Dyskeratosis congenitaEnrichmentPARN1.46
61Precursor t-cell acute lymphoblastic leukemiaEnrichmentCNOT31.38
62Fetal akinesia deformation sequence 1EnrichmentEXOSC31.37
63Parkinson disease, late-onsetEnrichmentEIF4G11.36
64Spastic ataxiaEnrichmentEXOSC81.22
65Myeloma, multipleEnrichmentDIS31.19
66Congenital nervous system abnormalityEnrichmentEXOSC30.93
67Nervous system diseaseEnrichmentEXOSC30.93
68MicrocephalyEnrichmentEXOSC30.87
69Ovarian cancerEnrichmentDICER10.77
70Inherited cancer-predisposing syndromeEnrichmentDICER10.66

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