1081
|
|
|
ATP synthase membrane subunit j |
6.8PL, ATP5MPL, C14orf2, MLQ, MP68, PLPM |
|
1082
|
|
|
ATP synthase membrane subunit k |
AGP, ATP5MD, DAPIT, HCVFTP2, MC5DN6, USMG5, bA792D24.4 |
|
1083
|
|
|
ATP synthase peripheral stalk-membrane subunit b |
ATP5F1, PIG47 |
|
1084
|
|
|
ATP synthase peripheral stalk subunit d |
APT5H, ATP5H, ATPQ |
|
1085
|
|
|
ATP synthase peripheral stalk subunit F6 |
ATP5, ATP5A, ATP5J, ATPM, CF6, F6 |
|
1086
|
|
|
ATP synthase peripheral stalk subunit OSCP |
ATP5O, ATPO, HMC08D05, MC5DN7, OSCP |
|
1087
|
|
|
Mitochondrially encoded ATP synthase 6 |
ATPase6, MTATP6 |
Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactylyView all (8 more) |
1088
|
|
|
- |
- |
Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactylyView all (8 more) |
1089
|
|
|
- |
- |
Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactylyView all (8 more) |
1090
|
|
|
ATPase H+ transporting accessory protein 1 |
16A, ATP6IP1, ATP6S1, Ac45, CF2, VATPS1, XAP-3, XAP3 |
|
