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Entry Name Description Category Pathway Gene
H02086 Mitochondrial complex III deficiency ... nine genes have been known to cause CIII deficiency. CYC1, UQCRB, UQCRQ, and UQCRC2 encode components of CIII itself, whereas BCS1L, TTC19, LYRM7, UQCC2, and UQCC3 produce mitochondrial assembly factors. Inherited metabolic disorder, Mitochondrial disease (MC3DN1) BCS1L [HSA:617] [KO:K08900]
(MC3DN2) TTC19 [HSA:54902] [KO:K18169]
(MC3DN3) UQCRB [HSA:7381] [KO:K00417]
(MC3DN4) UQCRQ [HSA:27089] [KO:K00418]
(MC3DN5) UQCRC2 [HSA:7385] [KO:K00415]
(MC3DN6) CYC1 [HSA:1537] [KO:K00413]
(MC3DN7) UQCC2 [HSA:84300] [KO:K17682]
(MC3DN8) LYRM7 [HSA:90624] [KO:K18170]
(MC3DN9) UQCC3 [HSA:790955] [KO:K23165]
(MC3DN10) UQCRFS1 [HSA:7386] [KO:K00411]
(MC3DN11) UQCRH [HSA:7388] [KO:K00416]
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