Mitochondrial translation

Pathway network for the Mitochondrial translation SuperPath

Sources:
  • Reactome

Pathways in the Mitochondrial translation SuperPath

#NameSourceGenes
1Mitochondrial translationReactome
2Mitochondrial translation terminationReactome
3Mitochondrial ribosome-associated quality controlReactome
4Mitochondrial translation initiationReactome
5Mitochondrial translation elongationReactome

Gene overlap in member pathways for Mitochondrial translation SuperPath

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

Disorders associated with Mitochondrial translation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Mitochondrial complex v deficiency, mitochondrial type 1EnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND516.00
2Neuropathy, ataxia, and retinitis pigmentosaEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND516.00
3Striatonigral degeneration, infantile, mitochondrialEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND516.00
4Camptodactyly of fingersEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND516.00
5Leigh syndrome, nuclearEnrichmentMRPS34, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND616.00
6Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND5, MT-ND616.00
7Leber hereditary optic neuropathy, modifier ofEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND616.00
8Leigh syndrome, mitochondrialEnrichmentMT-ATP6, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND5, MT-ND616.00
9Leber plus diseaseEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND616.00
10Mitochondrial myopathy with reversible cytochrome c oxidase deficiencyEnrichmentMT-ATP6, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND516.00
11Mitochondrial diseaseEnrichmentGFM2, MRPL39, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, OXA1L16.00
12HypertelorismEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND511.29
13Leigh diseaseEnrichmentMRPL39, MRPS34, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND611.27
14Mitochondrial myopathy, infantile, transientEnrichmentMT-ATP6, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND511.10
15Leber optic atrophy and dystoniaEnrichmentMT-ND1, MT-ND3, MT-ND4, MT-ND5, MT-ND610.66
16Retinitis pigmentosaEnrichmentMT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND56.31
17Familial colorectal cancerEnrichmentMT-CO1, MT-CO2, MT-CYB, MT-ND4L6.23
18Cardiomyopathy, infantile histiocytoidEnrichmentMT-ATP6, MT-ATP8, MT-CYB5.80
19Optic nerve diseaseEnrichmentMT-ATP6, MT-ATP8, MT-ND14.33
20Rare mitochondrial non-syndromic sensorineural deafnessEnrichmentMT-CO1, MT-ND1, MT-ND44.33
21Cardiomyopathy, infantile hypertrophicEnrichmentMT-ATP6, MT-ATP84.26
22Alzheimer disease mitochondrialEnrichmentMT-ND1, MT-ND24.26
23Periodic paralysis with later-onset distal motor neuropathyEnrichmentMT-ATP6, MT-ATP84.26
24Combined oxidative phosphorylation deficiency 1EnrichmentGFM1, MRPL443.92
25Perrault syndrome 1EnrichmentDAP3, ERAL1, MRPL493.87
26Cox deficiency, benign infantile mitochondrial myopathyEnrichmentMT-CO1, MT-CO2, MT-CO33.86
27Mitochondrial complex i deficiency, nuclear type 1EnrichmentMT-ND1, MT-ND2, MT-ND3, MT-ND43.75
28Hereditary recurrent myoglobinuriaEnrichmentMT-CO1, MT-CO33.49
29Optic atrophy plus syndromeEnrichmentMT-ND1, MT-ND4, MT-ND6, MTRFR3.33
30Mitochondrial complex iv deficiency, nuclear type 1EnrichmentMT-CO1, MT-CO2, MT-CO33.25
31Deafness, nonsyndromic sensorineural, mitochondrialEnrichmentMT-CO1, MT-ND13.09
32Parkinson disease 6, autosomal recessive early-onsetEnrichmentMT-ND5, MT-ND63.09
33Tetralogy of fallotEnrichmentMT-CO1, MT-CO2, MT-CO33.04
34Isolated atp synthase deficiencyEnrichmentMT-ATP6, MT-ATP82.83
35Aortic valve disease 1EnrichmentMT-ATP6, MT-ATP82.39
36Combined oxidative phosphorylation deficiency 2EnrichmentMRPS162.19
37Combined oxidative phosphorylation deficiency 34EnrichmentMRPS72.19
38Combined oxidative phosphorylation deficiency 51EnrichmentPTCD32.19
39Combined oxidative phosphorylation deficiency 16EnrichmentMRPL442.19
40Combined oxidative phosphorylation deficiency 5EnrichmentMRPS222.19
41Combined oxidative phosphorylation deficiency 15EnrichmentMTFMT2.19
42Combined oxidative phosphorylation deficiency 46EnrichmentMRPS232.19
43Mitochondrial complex i deficiency, nuclear type 27EnrichmentMTFMT2.19
44Combined oxidative phosphorylation deficiency 38EnrichmentMRPS142.19
45Ovarian dysgenesis 7EnrichmentMRPS222.19
46Combined oxidative phosphorylation deficiency 45EnrichmentMRPL122.19
47Combined oxidative phosphorylation deficiency 50EnrichmentMRPS252.19
48Combined oxidative phosphorylation deficiency 59EnrichmentMRPL392.19
49Perrault syndrome 7EnrichmentDAP32.19
50Combined oxidative phosphorylation deficiency 60EnrichmentMRPL492.19
51Combined oxidative phosphorylation deficiency 4EnrichmentTUFM2.19
52Combined oxidative phosphorylation deficiency 3EnrichmentTSFM2.19
53Spastic paraplegia 55, autosomal recessiveEnrichmentMTRFR2.18
54Combined oxidative phosphorylation deficiency 7EnrichmentMTRFR2.18
55Optic atrophy 14EnrichmentMIEF12.18
56Ataxia and polyneuropathy, adult-onsetEnrichmentMT-ATP62.13
57Mitochondrial complex i deficiency, mitochondrial type 1EnrichmentMT-ND32.13
58Myoglobinuria, recurrentEnrichmentMT-CO12.13
59Myopathy, lactic acidosis, and sideroblastic anemia 3EnrichmentMT-ATP62.13
60OncocytomaEnrichmentMT-ND62.13
61Combined oxidative phosphorylation deficiency 39EnrichmentGFM22.13
62Autosomal dominant spastic ataxiaEnrichmentMT-CO32.13
63Maternally-inherited spastic paraplegiaEnrichmentMT-ATP62.13
64Wilms tumor 2EnrichmentMRPL231.89
65Grange syndromeEnrichmentDAP31.89
66Waardenburg syndrome, type 2fEnrichmentMTFMT1.89
67Combined oxidative phosphorylation deficiency 36EnrichmentMRPS21.89
68Combined oxidative phosphorylation deficiency 47EnrichmentMRPS281.89
69Perrault syndrome 6EnrichmentERAL11.89
70Combined oxidative phosphorylation deficiency 9EnrichmentMRPL31.89
71Charcot-marie-tooth disease, demyelinating, type 1aEnrichmentMT-ATP61.83
72Deafness, sensorineural, autosomal-mitochondrial typeEnrichmentMT-ND11.83
73Charcot-marie-tooth disease type 1aEnrichmentMT-ATP61.83
74Combined oxidative phosphorylation deficiencyEnrichmentGFM11.72
75Neuropathy, hereditary motor and sensory, type via, with optic atrophyEnrichmentMTRFR1.71
76Keratoderma, palmoplantar, with deafnessEnrichmentMT-CO11.65
77Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathyEnrichmentMT-ND31.65
78Mitochondrial complex v deficiency, nuclear type 5EnrichmentMT-ND51.65
79Gonadal dysgenesisEnrichmentMT-ATP61.65
80Myelodysplastic syndrome with ring sideroblastsEnrichmentMT-CO11.65
81Combined oxidative phosphorylation deficiency 32EnrichmentMRPS341.59
82DystoniaEnrichmentMT-ND1, MT-ND61.56
83Familial infantile bilateral striatal necrosisEnrichmentMT-ATP61.53
84Mitochondrial oxidative phosphorylation disorderEnrichmentMTFMT1.50
85EpilepsyEnrichmentMT-CO3, MT-CYB1.45
86Kearns-sayre syndromeEnrichmentMT-ATP81.44
87ParkinsonismEnrichmentMT-ND61.29
88Perrault syndrome 2EnrichmentERAL11.25
89Mitochondrial encephalomyopathyEnrichmentMT-CYB1.14
9046 xx gonadal dysgenesisEnrichmentMRPS221.13
91Migraine with or without aura 1EnrichmentMT-ND11.10
92Isolated complex iii deficiencyEnrichmentMT-CYB1.10
93Premature menopauseEnrichmentMRPS71.10
94Myoclonic epilepsy associated with ragged-red fibersEnrichmentMT-ND51.07
95Restrictive cardiomyopathyEnrichmentMT-ND11.07
96Alzheimer's diseaseEnrichmentMT-ND11.03
97Beckwith-wiedemann syndromeEnrichmentMRPL230.96
98Hydrocephalus, congenital, 1EnrichmentMT-ND10.95
99Alzheimer disease, familial, 1EnrichmentMT-ND10.92
100Sudden infant death syndromeEnrichmentMT-ND10.92
101Parkinson's diseaseEnrichmentMT-ND10.88
102Colorectal cancerEnrichmentMT-CO1, MT-ND10.86
103Attention deficit-hyperactivity disorderEnrichmentMT-ND10.82
104Parkinson disease, late-onsetEnrichmentMT-ND10.78
105Auditory neuropathyEnrichmentMT-ND60.75
106Charcot-marie-tooth diseaseEnrichmentMT-ATP60.58
107Sensorineural hearing lossEnrichmentMRPS70.57
108Hereditary breast carcinomaEnrichmentMT-CYB0.55
109Body mass index quantitative trait locus 11EnrichmentMT-CYB0.51
110Primary ovarian insufficiencyEnrichmentMRPS70.50
111Dilated cardiomyopathyEnrichmentTSFM0.39
112Breast cancerEnrichmentMT-CYB0.37
113Rare genetic deafnessEnrichmentMT-ND10.35
114Ovarian cancerEnrichmentMT-CYB0.27
115Hereditary retinal dystrophyEnrichmentMT-ND4, MT-ND60.19
116Fundus dystrophyEnrichmentMT-ND4, MT-ND60.19

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