Processing of Capped Intronless Pre-mRNA

Pathway network for the Processing of Capped Intronless Pre-mRNA SuperPath

Sources:
  • Reactome

Pathways in the Processing of Capped Intronless Pre-mRNA SuperPath

#NameSourceGenes
1Processing of Capped Intronless Pre-mRNAReactome
2RNA Polymerase II Transcription TerminationReactome
3mRNA 3'-end processingReactome
4Processing of Intronless Pre-mRNAsReactome
5SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAsReactome
6SLBP independent Processing of Histone Pre-mRNAsReactome
7Inhibition of Host mRNA Processing and RNA SilencingReactome

Gene overlap in member pathways for Processing of Capped Intronless Pre-mRNA SuperPath

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

Disorders associated with Processing of Capped Intronless Pre-mRNA SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1InfluenzaDirect
2Aicardi-goutieres syndrome 8EnrichmentLSM113.13
3Cerebrocostomandibular syndromeEnrichmentSNRPB2.83
4Hypotrichosis 11EnrichmentSNRPE2.83
5Intellectual developmental disorder, x-linked 113EnrichmentCSTF22.83
6Pontocerebellar hypoplasia, type 10EnrichmentCLP12.83
7Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizuresEnrichmentCPSF32.83
8Neurodevelopmental disorder with hypotonia, microcephaly, and seizuresEnrichmentCPSF32.53
9Myopia 27, autosomal dominantEnrichmentCPSF12.53
10Chronic eosinophilic leukemiaEnrichmentFIP1L12.53
11Robin sequence with cleft mandible and limb anomaliesEnrichmentEIF4A32.37
12Intellectual developmental disorder, x-linked, syndromic 14EnrichmentUPF3B2.37
13Developmental delay, dysmorphic facies, and brain anomaliesEnrichmentU2AF22.37
14Arthrogryposis multiplex congenita 7, x-linkedEnrichmentTHOC22.37
15Pontocerebellar hypoplasia, type 15EnrichmentCDC402.37
16Retinitis pigmentosa 84EnrichmentDHX382.37
17Syndromic x-linked intellectual disability 14EnrichmentUPF3B2.37
18Deafness, autosomal dominant 86EnrichmentTHOC12.37
19Pierre robin syndromeEnrichmentSNRPB2.35
20Oculopharyngeal muscular dystrophy 1EnrichmentPABPN12.35
21Hypotrichosis simplexEnrichmentSNRPE2.18
22Aicardi-goutiares syndromeEnrichmentLSM112.18
23Primary hypereosinophilic syndromeEnrichmentFIP1L12.13
24Intellectual developmental disorder, x-linked, syndromic, kumar typeEnrichmentTHOC22.07
25Beaulieu-boycott-innes syndromeEnrichmentTHOC62.07
26Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalitiesEnrichmentSRSF12.07
27Immunodeficiency 127EnrichmentTHOC22.07
28Intellectual developmental disorder, x-linked, syndromic, lujan-fryns typeEnrichmentUPF3B1.89
29Thrombocytopenia-absent radius syndromeEnrichmentRBM8A1.89
30Chronic myelomonocytic leukemiaEnrichmentSRSF21.77
31Systemic mastocytosis with associated hematologic neoplasmEnrichmentSRSF21.77
32Acute promyelocytic leukemiaEnrichmentFIP1L11.72
33Aggressive systemic mastocytosisEnrichmentSRSF21.67
34Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentSRSF21.42
35Myelodysplastic syndromeEnrichmentU2AF11.34
36Pontocerebellar hypoplasiaEnrichmentCDC401.13
37LeukodystrophyEnrichmentU2AF21.09
38Non-syndromic x-linked intellectual disabilityEnrichmentUPF3B0.84
39Leukemia, acute myeloidEnrichmentSRSF20.80
40Complex neurodevelopmental disorderEnrichmentCPSF30.77
41Retinitis pigmentosaEnrichmentDHX380.22
42Hereditary retinal dystrophyEnrichmentDHX380.15
43Fundus dystrophyEnrichmentDHX380.15

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