1111
|
|
|
ATPase H+ transporting V1 subunit G1 |
ATP6G, ATP6G1, ATP6GL, ATP6J, Vma10 |
|
1112
|
|
|
ATPase H+ transporting V1 subunit G2 |
ATP6G, ATP6G2, NG38, VMA10 |
|
1113
|
|
|
ATPase H+ transporting V1 subunit G3 |
ATP6G3, Vma10 |
Bipolar disorder, Crohn disease, Hyperthyroidism, Inflammatory bowel disease, Insomnia, Obsessive-compulsive disorder, Optic atrophy, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis |
1114
|
|
|
ATPase H+ transporting V1 subunit H |
CGI-11, MSTP042, NBP1, SFD, SFDalpha, SFDbeta, VMA13 |
|
1115
|
|
|
ATPase copper transporting alpha |
DSMAX, HMNX, MK, MNK, SMAX3 |
Anemia, Aortic rupture, Ataxia, Au-kline syndrome, Charcot-marie-tooth disease, Colonic neoplasms, Cutis laxa, Ehlers-danlos syndrome, Growth disorder, Hemolysis, Hepatitis, Hereditary motor and sensory neuropathies, Hirschsprung disease, Pulmonary hypertension, Liver neoplasms, Distal hereditary motor neuropathy, Paralysis, Seizures, Spinal muscular atrophy, Tremor, Vascular system injury, X-linked distal spinal muscular atrophyView all (7 more) |
1116
|
|
|
ATPase copper transporting beta |
PWD, WC1, WD, WND |
Alzheimer disease, Anaptoglobinemia, Breast neoplasms, Carcinoma, Persistent hepatitis, Colorectal neoplasms, Congenital disorder of glycosylation, Deafness, Developmental and epileptic encephalopathy, Dyslexia, Fatty liver, Fatty liver, alcoholic, Hepatitis, Hepatolenticular degeneration, Kidney neoplasms, Liver cirrhosis, Liver disease, Liver failure, Liver neoplasms, Major depressive disorder, Intellectual developmental disorder, Mouth neoplasms, Neuropathy, Optic neuritis, Ovarian neoplasms, Prostatic neoplasms, Sensory peripheral neuropathy, Spastic ataxia, Squamous cell carcinoma, Testicular disease, Depression, Wilson diseaseView all (17 more) |
1117
|
|
|
Mitochondrially encoded ATP synthase 8 |
ATPase8, MTATP8 |
Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Periodic paralysis with later-onset distal motor neuropathy, Rod-cone dystrophy, Postaxial polydactyly |
1118
|
|
|
- |
- |
Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Periodic paralysis with later-onset distal motor neuropathy, Rod-cone dystrophy, Postaxial polydactyly |
1119
|
|
|
- |
- |
Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Periodic paralysis with later-onset distal motor neuropathy, Rod-cone dystrophy, Postaxial polydactyly |
1120
|
|
|
ATPase phospholipid transporting 8A1 |
ATPASEII, ATPIA, ATPP2 |
|
