rRNA processing in the nucleus and cytosol

Pathway network for the rRNA processing in the nucleus and cytosol SuperPath

Sources:
  • Reactome

Pathways in the rRNA processing in the nucleus and cytosol SuperPath

#NameSourceGenes
1rRNA processing in the nucleus and cytosolReactome
2rRNA processingReactome
3Major pathway of rRNA processing in the nucleolus and cytosolReactome
4rRNA modification in the nucleus and cytosolReactome

Gene overlap in member pathways for rRNA processing in the nucleus and cytosol SuperPath

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

Disorders associated with rRNA processing in the nucleus and cytosol SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Diamond-blackfan anemiaEnrichmentRPL11, RPL15, RPL17, RPL18, RPL26, RPL27, RPL31, RPL35, RPL35A, RPL5, RPL8, RPL9, RPS10, RPS15A, RPS17, RPS19, RPS20, RPS24, RPS26, RPS27, RPS28, RPS29, RPS716.00
2Diamond-blackfan anemia 1EnrichmentRPL11, RPL17, RPL35A, RPL5, RPL9, RPS10, RPS17, RPS19, RPS20, RPS24, RPS26, RPS710.93
3Pontocerebellar hypoplasia, type 1eEnrichmentEXOSC3, EXOSC8, EXOSC94.32
4Dyskeratosis congenitaEnrichmentDKC1, NHP2, NOP104.10
5Diamond-blackfan anemia 15 with mandibulofacial dysostosisEnrichmentRPS26, RPS283.26
6North american indian childhood cirrhosisEnrichmentUTP42.35
7Glaucoma 1, open angle, gEnrichmentWDR362.35
8Dyskeratosis congenita, autosomal recessive 1EnrichmentNOP102.35
9Bowen-conradi syndromeEnrichmentEMG12.35
1046,xy sex reversal 11EnrichmentDHX372.35
11Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2EnrichmentNOP102.35
12Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1EnrichmentDKC12.35
13Diamond-blackfan anemia 8EnrichmentRPS72.35
14Microcephaly 28, primary, autosomal recessiveEnrichmentRRP7A2.35
15Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomaliesEnrichmentDHX372.35
16Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9EnrichmentNOP102.35
17Chromosome 5q deletion syndromeEnrichmentRPS142.05
18Dyskeratosis congenita, autosomal recessive 2EnrichmentNHP22.05
19Neurodevelopmental disorder with speech delay and variable ocular anomaliesEnrichmentTHUMPD12.05
20Psychotic disorderEnrichmentRCL12.05
21Protein-deficiency anemiaEnrichmentRPL11, RPS261.89
22Aplasia cutis congenita, nonsyndromicEnrichmentBMS11.87
23Dyskeratosis congenita, x-linkedEnrichmentDKC11.87
24Congenital disorder of glycosylation, type ipEnrichmentUTP14C1.87
25Spinocerebellar ataxia 36EnrichmentNOP561.87
26Intellectual developmental disorder, x-linked, syndromic 35EnrichmentRPL101.87
27Asplenia, isolated congenitalEnrichmentRPSA1.87
28Intellectual developmental disorder, x-linked, syndromic, wilson-turner typeEnrichmentLAS1L1.87
29Diamond-blackfan anemia 10EnrichmentRPS261.87
30Alopecia, neurologic defects, and endocrinopathy syndromeEnrichmentRBM281.87
31Hypotrichosis 12EnrichmentRPL211.87
32Diamond-blackfan anemia 13EnrichmentRPS291.87
33Advanced sleep phase syndrome, familial, 2EnrichmentCSNK1D1.87
34Diamond-blackfan anemia 7EnrichmentRPL111.87
35Diamond-blackfan anemia 18EnrichmentRPL181.87
36Spondyloepimetaphyseal dysplasia, isidor-toutain typeEnrichmentRPL131.87
37Spermatogenic failure 63EnrichmentRPL10L1.87
38Pontocerebellar hypoplasia, type 1fEnrichmentEXOSC11.87
39Autism x-linked 5EnrichmentRPL101.87
40Cerebellar ataxia, brain abnormalities, and cardiac conduction defectsEnrichmentEXOSC51.87
41Diamond-blackfan anemia 20EnrichmentRPS15A1.87
42Hoxha-aliu syndromeEnrichmentERI11.87
43Diamond-blackfan anemia 3EnrichmentRPS241.87
44Diamond-blackfan anemia 4EnrichmentRPS171.87
45Diamond-blackfan anemia 11EnrichmentRPL261.87
46Pontocerebellar hypoplasia, type 1cEnrichmentEXOSC81.87
47Inflammatory poikiloderma with hair abnormalities and acral keratosesEnrichmentLTV11.87
48Spondyloepimetaphyseal dysplasiaEnrichmentRPL131.87
49Pontocerebellar hypoplasia, type 1dEnrichmentEXOSC91.87
50Diamond-blackfan anemia 19EnrichmentRPL351.87
51Short stature, hearing loss, retinitis pigmentosa, and distinctive faciesEnrichmentEXOSC21.87
52Brachycephaly, trichomegaly, and developmental delayEnrichmentRPS231.87
53Cardiomyopathy, dilated, 2dEnrichmentRPL3L1.87
54Spinal muscular atrophy with respiratory distress type 2EnrichmentLAS1L1.87
55X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndromeEnrichmentRPL101.87
56Spondyloepimetaphyseal dysplasia, guo-campeau typeEnrichmentERI11.87
57Pure red-cell aplasiaEnrichmentRPS261.87
58Diamond-blackfan anemia 22EnrichmentRPL171.87
59X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndromeEnrichmentRPL101.87
60Hsd10 mitochondrial diseaseEnrichmentHSD17B101.81
61Combined oxidative phosphorylation deficiency 30EnrichmentTRMT10C1.81
62Syndromic x-linked intellectual disability type 10EnrichmentHSD17B101.81
63Prostate cancer, hereditary, 2EnrichmentELAC21.81
64Combined oxidative phosphorylation deficiency 17EnrichmentELAC21.81
65Mitochondrial dna depletion syndrome 17EnrichmentMRM21.81
66Fastkd2-related infantile mitochondrial encephalomyopathyEnrichmentFASTKD21.81
67Aplasia cutis congenitaEnrichmentBMS11.65
68Pontocerebellar hypoplasiaEnrichmentEXOSC3, EXOSC91.61
69Coloboma of optic nerveEnrichmentDHX371.57
70Hoyeraal-hreidarsson syndromeEnrichmentDKC11.57
71Diamond-blackfan anemia 6EnrichmentRPL51.57
72Diamond-blackfan anemia 9EnrichmentRPS101.57
73Diamond-blackfan anemia 5EnrichmentRPL35A1.57
74Diamond-blackfan anemia 12EnrichmentRPL151.57
75Wilson-turner syndromeEnrichmentLAS1L1.57
76Diamond-blackfan anemia 16EnrichmentRPL271.57
77Diamond-blackfan anemia 17EnrichmentRPS271.57
78Congenital pontocerebellar hypoplasia type 1EnrichmentEXOSC31.57
79Familial isolated congenital aspleniaEnrichmentRPSA1.57
80Combined oxidative phosphorylation deficiency 54EnrichmentPRORP1.51
81Combined oxidative phosphorylation deficiency 44EnrichmentFASTKD21.51
82Spastic ataxia 10, autosomal recessiveEnrichmentTRUB21.51
83Pontocerebellar hypoplasia, type 1bEnrichmentEXOSC31.40
84Cerebellar diseaseEnrichmentEXOSC31.40
85Macrocytic anemiaEnrichmentRPL171.40
86Advanced sleep phase syndromeEnrichmentCSNK1D1.40
87PolymicrogyriaEnrichmentDHX371.36
88Coenzyme q10 deficiency, primary, 7EnrichmentTRUB21.34
8946,xy complete gonadal dysgenesisEnrichmentDHX371.32
9046,xy partial gonadal dysgenesisEnrichmentDHX371.21
91Male infertility with spermatogenesis disorderEnrichmentDHX371.18
92HemangiomaEnrichmentRPL51.18
93Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentDKC11.16
94PancytopeniaEnrichmentRPL171.10
95Williams-beuren syndromeEnrichmentBUD231.06
96Hypotrichosis simplexEnrichmentRPL210.94
97Leukemia, chronic lymphocyticEnrichmentRPS150.89
98Aplastic anemiaEnrichmentRPL50.89
99Perrault syndrome 2EnrichmentPRORP0.88
100Atrial heart septal defectEnrichmentRPL50.86
101Interatrial communicationEnrichmentRPL50.86
102Familial colorectal cancer type xEnrichmentRPS200.86
103Rare mitochondrial non-syndromic sensorineural deafnessEnrichmentTFB1M0.84
104EpicanthusEnrichmentRPL170.82
105Renal hypodysplasia/aplasia 3EnrichmentERI10.82
106Pulmonary hypertension, primary, 1EnrichmentRPL50.79
107Lactic acidosisEnrichmentPRORP0.77
108Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentDHX37, RPL10L0.75
109Perrault syndrome 1EnrichmentPRORP0.65
110Congenital myopathyEnrichmentEXOSC30.64
111LissencephalyEnrichmentEXOSC30.60
112Attention deficit-hyperactivity disorderEnrichmentRPL170.59
113Developmental and epileptic encephalopathy 1EnrichmentCSNK1E0.54
114Mitochondrial complex iv deficiency, nuclear type 1EnrichmentFASTKD20.53
115Prostate cancerEnrichmentELAC20.44
116Fetal akinesia deformation sequence 1EnrichmentEXOSC30.40
117West syndromeEnrichmentCSNK1E0.34
118Spastic ataxiaEnrichmentEXOSC80.29
119Familial isolated dilated cardiomyopathyEnrichmentRPL3L0.29
120Myeloma, multipleEnrichmentDIS30.27
121MicrocephalyEnrichmentEXOSC3, PRORP0.24
122AutismEnrichmentRPL170.20
123Leigh syndrome, nuclearEnrichmentFASTKD20.18
124Leigh diseaseEnrichmentFASTKD20.16
125Mitochondrial diseaseEnrichmentTRMT10C0.13
126Congenital nervous system abnormalityEnrichmentEXOSC30.12
127Nervous system diseaseEnrichmentEXOSC30.12
128Ovarian cancerEnrichmentELAC20.10
129Inherited cancer-predisposing syndromeEnrichmentRPS200.08

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