4111
|
|
|
Mitochondrial transcription rescue factor 1 |
C6orf203, HSPC230, PRED31 |
Curated: Prostate cancer, Hypertension
Unreviewed: N/A
|
4112
|
|
|
MTRES1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4113
|
|
|
MTRES1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
4114
|
|
|
Mtr4 exosome RNA helicase |
Dob1, KIAA0052, Mtr4, SKIV2L2, fSAP118 |
Curated: N/A
Unreviewed: Amyotrophic lateral sclerosis, Cardiomyopathy, Cervical Intraepithelial Neoplasia, Cervix carcinoma, Coronary artery disease, Lupus Erythematosus, Lymphoma, Myeloid leukemia
|
4115
|
|
|
Mitochondrial translation release factor 1 |
MRF1, MTTRF1, RF1 |
Curated: Cardiovascular disease
Unreviewed: Kidney Disease, Kidney Failure
|
4116
|
|
|
Mitochondrial translation release factor 1 like |
HMRF1L, MRF1L, mtRF1a |
Curated: N/A
Unreviewed: N/A
|
4117
|
|
|
Mitochondrial translational release factor 1 like pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4118
|
|
|
Mitochondrial translational release factor 1 like pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
4119
|
|
|
Mitochondrial translation release factor in rescue |
C12orf65, COXPD7, SPG55, mtRF-R |
Curated: Alzheimer disease, Asthma, Spastic paraplegia, Combined oxidative phosphorylation deficiency, Endometriosis, Developmental and epileptic encephalopathy, Hereditary motor and sensory neuropathies, Leigh syndrome, Metabolic syndrome, Mitochondrial disease, Mitochondrial encephalomyopathy, Neurodevelopmental disorder, Optic atrophy, Osteoarthritis, Retinitis pigmentosa, Schizophrenia, Hereditary spastic paraplegia, Diabetes mellitus type 2, Uterine fibroid
Unreviewed: Arthrogryposis multiplex congenita, Cognition disorder, Combined Oxidative Phosphorylation Deficiency, Congenital Clubfoot, Developmental Delay, Developmental regression, Dysarthria, Epileptic encephalopathy, Hypoplasia Of Corpus Callosum, Impaired Cognition, Intellectual developmental disorder, Leigh Syndrome, Mental retardation, Mitochondrial Diseases, Movement Disorders, Nervous System Diseases, Neuropathy, Nystagmus, Ophthalmoplegia, Optic Atrophy, Paralytic Ileus, Paraparesis, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polyneuropathy, Ptosis, Rheumatoid arthritis, Spastic Paraplegia, Strabismus
|
4120
|
|
|
MT-RNR2 like 1 (pseudogene) |
HN1, RNA143598 |
Curated: N/A
Unreviewed: Dyslipidemias, Ovarian neoplasm
|