Translation factors

Pathway network for the Translation factors SuperPath

Sources:
  • WikiPathways
  • Reactome

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

Disorders associated with Translation factors SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Leukoencephalopathy with vanishing white matter 1EnrichmentEIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B510.55
2Leukoencephalopathy with vanishing white matter 5EnrichmentEIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B510.37
3Leukoencephalopathy with vanishing white matterEnrichmentEIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B510.26
4Mehmo syndromeEnrichmentEIF2S33.23
5Leukoencephalopathy with vanishing white matter 3EnrichmentEIF2B33.23
6Leukoencephalopathy with vanishing white matter 2EnrichmentEIF2B23.23
7Leukoencephalopathy with vanishing white matter 4EnrichmentEIF2B42.93
8Intellectual developmental disorder, autosomal recessive 67EnrichmentEIF3F2.63
9Parkinson disease 18, autosomal dominantEnrichmentEIF4G12.43
10Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent languageEnrichmentEEF1D2.43
11Leukoencephalopathy, developmental delay, and episodic neurologic regression syndromeEnrichmentEIF2AK22.43
12Autism 19EnrichmentEIF4E2.43
13Leukoencephalopathy, motor delay, spasticity, and dysarthria syndromeEnrichmentEIF2AK12.43
14Spinocerebellar ataxia 26EnrichmentEEF22.43
15Neurodevelopmental disorder with hypotonia and speech delay, with or without seizuresEnrichmentEIF4A22.43
16Intellectual developmental disorder, autosomal dominant 38EnrichmentEEF1A22.43
17Faundes-banka syndromeEnrichmentEIF5A2.43
18Dystonia 33EnrichmentEIF2AK22.43
19Chromosome 5q deletion syndromeEnrichmentEEF1D2.13
20Epiphyseal dysplasia, multiple, with early-onset diabetes mellitusEnrichmentEIF2AK32.13
21Developmental and epileptic encephalopathy 33EnrichmentEEF1A22.13
22Leukodystrophy, hypomyelinating, 17EnrichmentEIF2AK12.13
23Spastic paraplegia 46, autosomal recessiveEnrichmentEEF1A22.13
24Premature menopauseEnrichmentEIF2B22.12
25Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentEIF3F1.98
26Menkes diseaseEnrichmentEIF2AK31.96
27Heparin cofactor ii deficiencyEnrichmentEIF4G31.96
28Torsion dystonia 1EnrichmentEIF2AK21.96
29Brittle bone disorderEnrichmentEIF2B21.87
30Autosomal recessive non-syndromic intellectual disabilityEnrichmentEEF1B2, EEF1D1.71
31Autosomal recessive intellectual developmental disorderEnrichmentEEF1D1.66
32Hereditary breast ovarian cancer syndromeEnrichmentEIF2B51.50
33Differentiated thyroid carcinomaEnrichmentEIF1AX1.47
34Primary ovarian insufficiencyEnrichmentEIF2B21.46
35Congenital nervous system abnormalityEnrichmentEIF2B21.22
36Nervous system diseaseEnrichmentEIF2B21.22
37Myeloma, multipleEnrichmentEIF1AX1.19
38Williams-beuren syndromeEnrichmentEIF4H1.15
39Complex neurodevelopmental disorderEnrichmentEIF4A2, EIF5A1.12
40Parkinson disease, late-onsetEnrichmentEIF4G11.07
41Autosomal dominant non-syndromic intellectual disabilityEnrichmentEEF1A20.77
42Undetermined early-onset epileptic encephalopathyEnrichmentEEF1A20.73
43AutismEnrichmentGSPT20.63

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