811
|
|
|
MICOS10 pseudogene 3 |
MINOS1P3 |
Curated: N/A
Unreviewed: N/A
|
812
|
|
|
MICOS10 pseudogene 4 |
MINOS1P4 |
Curated: N/A
Unreviewed: N/A
|
813
|
|
|
Mitochondrial contact site and cristae organizing system subunit 13 |
C19orf70, MIC12, MIC13, P117, QIL1 |
Curated: 3-methylglutaconic aciduria, Combined oxidative phosphorylation deficiency, Mitochondrial disease
Unreviewed: Brain disease, Cerebellar atrophy, Choreoathetosis, Developmental Delay, Dysarthria, Hearing Loss, Hypoglycemia, Liver disease, Mental retardation, Mitochondrial Diseases, Mitochondrial encephalopathy, Neurodegenerative disorder, Nystagmus, Optic Atrophy, Respiratory Failure, Spinocerebellar ataxia, Ventricular arrhythmia, Visceral neuropathy
|
814
|
|
|
Mitochondrial calcium uptake 1 |
CALC, CBARA1, EFHA3, MPXPS, ara CALC |
Curated: Atrial fibrillation, Basal ganglia disease, Congenital neurologic anomalies, Learning disorders, Mitochondrial disease, Movement disorder, Myopathy, Neurodevelopmental disorder, Sarcoidosis
Unreviewed: Anemia, Anophthalmia, Arteriosclerosis, Atherosclerosis, Basal Ganglia Diseases, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cognition disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetic cardiomyopathy, Extrapyramidal disease, Hyperglycemia, Hyperlipidemia, Impaired Cognition, Learning Disorders, Lenticulostriate Disorders, Malignant Neoplasm, Melanoma, Microcephaly, Motor delay, Movement Disorders, Myopathy With Extrapyramidal Signs, Neoplasms, Nervous System Disorder, Neuromuscular Diseases, Optic Atrophy, Orofacial dyskinesia, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Parkinson disease, Peripheral axonal neuropathy, Prostate cancer, Proximal myopathy with extrapyramidal signs, Ptosis, Septicemia, Sleep deprivation, Specific Learning Disorder, Squamous cell carcinoma, Status marmoratus
|
815
|
|
|
Mitochondrial calcium uptake 2 |
1110008L20Rik, EFHA1, hMICU3 |
Curated: Atrial fibrillation, Mitochondrial disease
Unreviewed: Impaired Cognition, Neurodevelopmental Disorders, Parkinson disease, Squamous cell carcinoma
|
816
|
|
|
Mitochondrial calcium uptake 3 |
EFHA2, hMICU3 |
Curated: Obstructive pulmonary disease
Unreviewed: Stomach neoplasms
|
817
|
|
|
Midline 1 |
BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY |
Curated: Alzheimer disease, Clinodactyly, Congenital esophageal anomaly, Dandy-walker syndrome, X-linked opitz syndrome
Unreviewed: N/A
|
818
|
|
|
MID1 interacting protein 1 |
G12-like, MIG12, S14R, STRAIT11499, THRSPL |
Curated: N/A
Unreviewed: Androgen-Insensitivity Syndrome, Colorectal neoplasm, Fatty Liver, Hepatocellular carcinoma, Hyperlipidemia, Opitz GBBB Syndrome, X-Linked, Thyroid cancer
|
819
|
|
|
MID1IP1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
820
|
|
|
Midline 2 |
FXY2, MRX101, RNF60, TRIM1, XLID101 |
Curated: Esophageal atresia, Intellectual developmental disorder, x-linked, X-linked intellectual disability
Unreviewed: Asthma, Attention Deficit Hyperactivity Disorder, Autism, Carcinogenesis, Developmental Delay, Developmental disability, Facial paralysis, FG Syndrome, Intellectual developmental disorder, Macrocephaly, Meckel Diverticulum, Mental retardation, Mental Retardation, X-Linked, Mouth neoplasm, Neurosensory Hearing impairment, Non-Syndromic Intellectual Disability, X-Linked, Obesity, Opitz GBBB syndrome, Opitz GBBB Syndrome, X-Linked, Ovarian neoplasm, Parkinson disease, Seizure, Strabismus, Syndactyly Of The Toes
|