Complex III assembly

No Pathway Network information available for Complex III assembly

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

Disorders associated with Complex III assembly SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Isolated complex iii deficiencyEnrichmentBCS1L, CYC1, LYRM7, MT-CYB, TTC19, UQCC2, UQCC3, UQCRB, UQCRC2, UQCRFS1, UQCRQ16.00
2Mitochondrial complex iii deficiency, nuclear type 1EnrichmentBCS1L, LYRM75.47
3Combined oxidative phosphorylation deficiency 19EnrichmentLYRM4, NFS14.98
4Mitochondrial diseaseEnrichmentMT-CYB, TTC19, UQCRC23.23
5Mitochondrial complex iii deficiency, nuclear type 3EnrichmentUQCRB2.96
6Mitochondrial complex iii deficiency, nuclear type 6EnrichmentCYC12.96
7Mitochondrial complex iii deficiency, nuclear type 7EnrichmentUQCC22.96
8Bjornstad syndromeEnrichmentBCS1L2.96
9Gracile syndromeEnrichmentBCS1L2.96
10Mitochondrial complex iii deficiency, nuclear type 8EnrichmentLYRM72.96
11Mitochondrial complex iii deficiency, nuclear type 10EnrichmentUQCRFS12.96
12Mitochondrial complex iii deficiency, nuclear type 11EnrichmentUQCRH2.96
13Renal tubulopathy-encephalopathy-liver failure syndromeEnrichmentBCS1L2.96
14Myopathy with lactic acidosis, hereditaryEnrichmentISCU2.72
15Even-plus syndromeEnrichmentHSPA92.72
16Anemia, sideroblastic, 4EnrichmentHSPA92.72
17Combined oxidative phosphorylation deficiency 52EnrichmentNFS12.72
18Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunctionEnrichmentLETM12.72
19Anemia, sideroblastic, 5EnrichmentHSCB2.72
20Mitochondrial complex iii deficiency, nuclear type 9EnrichmentUQCC32.66
21Parkinsonism with polyneuropathyEnrichmentUQCRC12.66
22Mitochondrial complex iii deficiency, nuclear type 2EnrichmentTTC192.48
23Autosomal recessive sideroblastic anemiaEnrichmentHSPA92.42
24Propionic acidemiaEnrichmentUQCRFS12.35
25Mitochondrial complex v deficiency, nuclear type 3EnrichmentUQCRC22.35
26Mitochondrial complex iii deficiency, nuclear type 4EnrichmentUQCRQ2.26
27Friedreich ataxiaEnrichmentFXN2.24
28Cardiomyopathy, infantile histiocytoidEnrichmentMT-CYB2.12
29Leigh syndrome, nuclearEnrichmentBCS1L, MT-CYB2.12
30Leigh diseaseEnrichmentBCS1L, MT-CYB2.03
31Wolf-hirschhorn syndromeEnrichmentLETM11.94
32Movement diseaseEnrichmentBCS1L1.92
33Lactic acidosisEnrichmentUQCRFS11.88
34Mitochondrial myopathy, infantile, transientEnrichmentMT-CYB1.77
35Mitochondrial encephalomyopathyEnrichmentMT-CYB1.72
36Familial colorectal cancerEnrichmentMT-CYB1.72
37Mitochondrial myopathy with reversible cytochrome c oxidase deficiencyEnrichmentMT-CYB1.72
38Hypertrophic cardiomyopathyEnrichmentUQCRC11.33
39Leber hereditary optic neuropathy, modifier ofEnrichmentMT-CYB1.16
40Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesEnrichmentMT-CYB1.15
41EpilepsyEnrichmentMT-CYB1.13
42Hereditary breast carcinomaEnrichmentMT-CYB1.09
43Body mass index quantitative trait locus 11EnrichmentMT-CYB1.04
44MicrocephalyEnrichmentBCS1L0.89
45Breast cancerEnrichmentMT-CYB0.87
46Leber plus diseaseEnrichmentMT-CYB0.78
47Ovarian cancerEnrichmentMT-CYB0.75

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