Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S

Pathway network for the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S SuperPath

Sources:
  • Reactome

Pathways in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S SuperPath

#NameSourceGenes
1Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43SReactome
2Translation initiation complex formationReactome
3Ribosomal scanning and start codon recognitionReactome
4Formation of the ternary complex, and subsequently, the 43S complexReactome

Gene overlap in member pathways for Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S SuperPath

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

Disorders associated with Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Diamond-blackfan anemiaEnrichmentRPS10, RPS15A, RPS17, RPS19, RPS20, RPS24, RPS26, RPS27, RPS28, RPS29, RPS711.07
2Diamond-blackfan anemia 1EnrichmentRPS10, RPS17, RPS19, RPS20, RPS24, RPS26, RPS710.78
3Diamond-blackfan anemia 15 with mandibulofacial dysostosisEnrichmentRPS26, RPS284.37
4Asplenia, isolated congenitalEnrichmentRPSA2.42
5Diamond-blackfan anemia 10EnrichmentRPS262.42
6Diamond-blackfan anemia 13EnrichmentRPS292.42
7Mehmo syndromeEnrichmentEIF2S32.42
8Diamond-blackfan anemia 20EnrichmentRPS15A2.42
9Diamond-blackfan anemia 3EnrichmentRPS242.42
10Diamond-blackfan anemia 8EnrichmentRPS72.42
11Diamond-blackfan anemia 4EnrichmentRPS172.42
12Brachycephaly, trichomegaly, and developmental delayEnrichmentRPS232.42
13Pure red-cell aplasiaEnrichmentRPS262.42
14Parkinson disease 18, autosomal dominantEnrichmentEIF4G12.36
15Autism 19EnrichmentEIF4E2.36
16Neurodevelopmental disorder with hypotonia and speech delay, with or without seizuresEnrichmentEIF4A22.36
17Chromosome 5q deletion syndromeEnrichmentRPS142.12
18Diamond-blackfan anemia 9EnrichmentRPS102.12
19Intellectual developmental disorder, autosomal recessive 67EnrichmentEIF3F2.12
20Diamond-blackfan anemia 17EnrichmentRPS272.12
21Familial isolated congenital aspleniaEnrichmentRPSA2.12
22Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentEIF3F1.47
23Leukemia, chronic lymphocyticEnrichmentRPS151.42
24Familial colorectal cancer type xEnrichmentRPS201.38
25Protein-deficiency anemiaEnrichmentRPS261.31
26Williams-beuren syndromeEnrichmentEIF4H1.08
27Parkinson disease, late-onsetEnrichmentEIF4G11.00
28Differentiated thyroid carcinomaEnrichmentEIF1AX0.98
29Myeloma, multipleEnrichmentEIF1AX0.71
30Inherited cancer-predisposing syndromeEnrichmentRPS200.40
31Complex neurodevelopmental disorderEnrichmentEIF4A20.38

Loading...
Loading...
Loading...