|
211
|
|
|
Mediator complex subunit 13L |
MRFACD, PROSIT240, THRAP2, TRAP240L |
Autism, Breast cancer, Cardiac anomalies - developmental delay - facial dysmorphism syndrome, Central nervous system cancer, Congenital camptodactyly, Congenital heart disease, Corneal astigmatism, Crohn disease, Melanoma, Developmental delay, Developmental delay with facial dysmorphism syndrome, Glioblastoma, Glioma, Global developmental delay, Inflammatory bowel disease, Intellectual developmental disorder, Intellectual disability, Neurodevelopmental disorders, Scoliosis, Strabismus, Vesicoureteral refluxView all (6 more) |
|
212
|
|
|
Malonyl-CoA decarboxylase |
MCD |
|
|
213
|
|
|
Microtubule actin crosslinking factor 1 |
ABP620, ACF7, KIAA0754, LIS9, Lnc-PMIF, MACF, OFC4 |
Alzheimer disease, Anorexia nervosa, Isolated sensorineural deafness, Nonsyndromic hearing loss, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Colorectal cancer, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Global developmental delay, Lissencephaly, Metabolic syndrome, Migraine, Peripheral arterial disease, Schizophrenia, Sleep apnea, Diabetes mellitus, type 2, Type 2 diabetes nephropathyView all (4 more) |
|
214
|
|
|
MAF bZIP transcription factor F |
U-MAF, hMafF |
Juvenile arthritis, Basal cell carcinoma, Diabetes mellitus, Diverticular disease, Juvenile idiopathic arthritis, Melanocytic nevus, Metabolic syndrome, Oligoarticular juvenile idiopathic arthritis, Pelvic organ prolapse, Diabetes mellitus, type 2, Uterine prolapse |
|
215
|
|
|
Mitochondrial carrier 2 |
HSPC032, MIMP, SLC25A50 |
Diabetic eye disease, Diabetic retinopathy, Hemorrhoid, Hypertension, Insomnia, Major depressive disorder, Mood disorder, Neurotic disorder, Obesity, Diabetes mellitus, type 2 |
|
216
|
|
|
Mechanistic target of rapamycin kinase |
FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS |
Breast neoplasm, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Renal cell carcinoma, Small cell carcinoma, Cebalid syndrome, Colonic neoplasm, Diabetes mellitus type 2, Endocrine system disease, Focal cortical dysplasia, Glioblastoma, Hemimegalencephaly, Hepatomegaly, Hypertension, Hypertrophy, Intellectual developmental disorder, Left ventricular disease, Lymphatic metastasis, Major depressive disorder, Cortical development malformation, Mesothelioma, Depression, Neurodevelopmental disorders, Open angle glaucoma, Ovarian neoplasm, Polycystic kidney disease, Prostatic neoplasm, Pulmonary fibrosis, Schizophrenia, Intellectual disability, Diabetes mellitus, type 2, Urinary bladder cancer, Uterine fibroidView all (18 more) |
|
217
|
|
|
MMS22 like, DNA repair protein |
C6orf167, dJ39B17.2 |
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Digestive system disease, Diverticular disease, Gastroesophageal reflux disease, Lung cancer, Ovarian epithelial cancer, Metabolic syndrome, Multiple sclerosis, Neurotic disorder, Obstructive sleep apnea syndrome, Ovarian cancer, Schizophrenia, Tourette syndrome, Diabetes mellitus, type 2View all (2 more) |
|
218
|
|
|
Methionine sulfoxide reductase B3 |
DFNB74 |
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Central nervous system cancer, Deafness, Glioblastoma, Glioma, Hearing impairment, Hearing loss, Non-small cell lung carcinoma, Obstructive sleep apnea syndrome, Nonsyndromic hearing loss, Sleep apnea |
|
219
|
|
|
Methionyl aminopeptidase type 1D, mitochondrial |
MAP 1D, MAP1D, MetAP 1D, Metap1l |
|
|
220
|
|
|
Minichromosome maintenance 9 homologous recombination repair factor |
C6orf61, MCMDC1, ODG4, dJ329L24.1, dJ329L24.3 |
|
