5681
|
|
|
COP9 signalosome subunit 8 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
5682
|
|
|
COP9 signalosome subunit 8 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
5683
|
|
|
COP9 signalosome subunit 9 |
CSNAP, MYEOV2 |
Curated: N/A
Unreviewed: Triple negative breast cancer
|
5684
|
|
|
Coat protein complex I subunit zeta 1 |
CGI-120, COPZ, HSPC181, zeta-COP, zeta1-COP |
Curated: Venous thromboembolism
Unreviewed: Carcinogenesis, Cognition disorder, Glioblastoma, Glioma, Hepatocellular carcinoma, Hypoxia, Impaired Cognition, Neoplasms, Parkinson disease, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Uterine neoplasm
|
5685
|
|
|
Coat protein complex I subunit zeta 2 |
zeta2-COP |
Curated: Bell's palsy, Osteoarthritis, Prostate cancer
Unreviewed: Breast neoplasm, Endometrial Cancer, Endometrial carcinoma, Neoplasms, Thyroid cancer, Triple negative breast cancer, Urinary bladder neoplasms
|
5686
|
|
|
Coenzyme Q10A |
- |
Curated: Coronary artery disease, Psoriasis, Diabetes mellitus type 2
Unreviewed: N/A
|
5687
|
|
|
Coenzyme Q10B |
- |
Curated: Schizophrenia
Unreviewed: N/A
|
5688
|
|
|
Coenzyme Q10B pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
5689
|
|
|
Coenzyme Q10B pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
5690
|
|
|
Coenzyme Q2, polyprenyltransferase |
CL640, COQ10D1, MSA1, PHB:PPT |
Curated: Coenzyme q10 deficiency, Focal glomerulosclerosis, Kidney disease, Leigh syndrome, Mitochondrial disease, Multiple system atrophy, Nephrotic syndrome, Shy-drager syndrome, Systemic lupus erythematosus, Primary coenzyme q10 deficiency
Unreviewed: Alport Syndrome, Amyotrophic Lateral Sclerosis, Anemia, Anhidrosis, Anxiety Disorder, Bilateral convulsive seizures, Brain disease, Camptocormia, Central Visual Impairment, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar diseases, Cerebral Atrophy, Coenzyme Q10 Deficiency, Developmental regression, Dysarthria, Dysautonomia, Dystonia, Epileptic encephalopathy, Erectile Dysfunction, Female anorgasmia, Focal segmental glomerulosclerosis, Glomerulonephritis, Glomerulosclerosis, Hearing Loss, Hypertrophic cardiomyopathy, Hypoalbuminemia, Hypogonadism, Hypohidrosis, Intestinal Volvulus, Kidney Disease, Kidney failure, Leigh Syndrome With Nephrotic Syndrome, Lissencephaly, Liver failure, Mental Depression, Mental retardation, Metabolic Myopathy, Mitochondrial encephalomyopathy, Motor delay, Multiple System Atrophy, Myoclonic Epilepsy, Myopathy, Myositis, Nephritis, Nephrotic Syndrome, Neurodegenerative Disorders, Neuromuscular Diseases, Neuromuscular dysphagia, Nystagmus, Olivopontocerebellar Atrophies, Optic atrophy, Orofacial dyskinesia, Orthostatic syncope, Pancytopenia, Parkinson disease, Ptosis, Raynaud Phenomenon, Renal cyst, Renal Glomerular Disease, Rod-cone dystrophy, Senior-loken syndrome, Sleep Apnea, Specific Learning Disorder, Spinocerebellar Ataxia, Steroid resistant nephrotic syndrome, Striatonigral Degeneration
|