711
|
|
|
MFN1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
712
|
|
|
Mitofusin 2 |
CMT2A, CMT2A2, CMT2A2A, CMT2A2B, CPRP1, HMSN6A, HSG, MARF, MSL |
Curated: Amyotrophic lateral sclerosis, Autoimmune neurological syndrome, Eczema, Auditory neuropathy, Charcot-marie-tooth disease, Axonal hereditary motor and sensory neuropathy, Cardiomegaly, Cerebellar ataxia, Cerebral palsy, Dejerine-sottas disease, Diabetic neuropathy, Nail dystrophy, Global developmental delay, Hereditary motor and sensory neuropathies, Motor neuron disease, Hyperalgesia, Hypertrophic neuropathy, Inflammatory skin disease, Multiple system atrophy, Hereditary motor and sensory neuropathy, Optic atrophy, Peripheral neuropathy, Peroneal muscle atrophy, Psoriasis, Retinitis pigmentosa, Roussy-levy syndrome, Ventricular remodeling, multiple symmetric lipomatosis with partial lipodystrophy, Charcot-Marie-Tooth disease type 2A2
Unreviewed: Adenocarcinoma, Agenesis Of Corpus Callosum, Alzheimer disease, Amyotrophic Lateral Sclerosis, Anemia, Aortic dissection, Arteriosclerosis, Asthenozoospermia, Ataxia, Atherosclerosis, Atrophy of the spinal cord, Autism, Axonal Neuropathy, B-Cell Lymphoma, Benign Prostatic Hyperplasia, Bipolar disorder, Bladder carcinoma, Bladder Neoplasm, Blindness, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiac injury, Cardiomyopathy, Cardiovascular Diseases, Cartilage disease, Cataract, Cerebral Ischemia, Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Charcot-Marie-Tooth Disease, Cholelithiasis, Chronic Obstructive Pulmonary Disease, Cirrhosis, Cognition disorder, Cognitive disorder, Colorectal Cancer, Colorectal neoplasm, Congenital Cataract, Congenital glaucoma, Congestive Heart Failure, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Deafness, Demyelinating diseases, Dermatitis, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Diabetic Retinopathy, Dilated cardiomyopathy, Disorder Of Eye, Distal amyotrophy, Distal hereditary motor neuropathy, Distal lower limb amyotrophy, Drachtman Weinblatt Sitarz syndrome, Dysautonomia, Emery dreifuss muscular dystrophy, Eye disease, Fatty Liver, Friedreich Ataxia, Fuchs Endothelial Dystrophy, Gestational diabetes, Giant axonal neuropathy, Glaucoma, Glioblastoma, Glomerulosclerosis, Headache, Hearing Loss, Heart Failure, Hepatic Encephalopathy, Hepatocellular carcinoma, Hereditary Leber Optic Atrophy, Hereditary Liability To Pressure Palsies, Hereditary Motor And Sensory Neuropathy With Optic Atrophy, Hereditary sensory and autonomic neuropathy, Hereditary sensory and motor neuropathy, Huntington Disease, Hydrocephalus, Hyperplasia, Hypertension, Hypoxia, Inherited Peripheral Neuropathy, Intellectual developmental disorder, Interstitial Cystitis, Kidney disease, Kidney neoplasm, Leprosy, Leukemia, Lipoatrophy, Lipodystrophy, Lipomatosis, Liver Cancer, Liver carcinoma, Liver Cirrhosis, Liver disease, Liver failure, Liver Fibrosis, Liver neoplasms, Low Tension Glaucoma, Lung adenocarcinoma, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Malignant neoplasm of salivary gland, Melanoma, Mental retardation, Microphthalmos, Miscarriage, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial Respiratory Chain Deficiencies, Motor nerve neuritis, Motor Neuron Disease, Multiple Lipomata, Multiple Sclerosis, Multiple Symmetric Lipomatosis, Myeloid leukemia, Myocardial Ischemia, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neurogenic bladder, Neuropathy, Neuropathy Ataxia And Retinis Pigmentosa, Non-Alcoholic Fatty Liver Disease, Nyctalopia, Obesity, Optic Atrophy, Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy, Optic Neuropathy, Osteoarthritis, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Parkinson disease, Partial Paralysis Vocal Cords, Pelvic Organ Prolapse, Peripheral axonal atrophy, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polycystic kidney disease, Polyneuropathy, Prostate cancer, Proteinuria, Pulmonary arterial hypertension, Pulmonary Fibrosis, Renal cell carcinoma, Renal fibrosis, Respiratory system infectious disease, Restless Legs Syndrome, Restrictive cardiomyopathy, Retinal Diseases, Saxonal Neuropathy, Scoliosis, Sensory neuropathy, Sepsis, Septicemia, Sjogren syndrome, Sleep deprivation, Spastic Paraplegia, Spinal muscular atrophy, Stomach Carcinoma, Stomach Neoplasms, Stroke, Urinary bladder cancer, Vascular calcification, Vocal Cord Paralysis, Willis-ekbom disease
|
713
|
|
|
MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase |
- |
Curated: N/A
Unreviewed: Osteosarcoma
|
714
|
|
|
Membrane frizzled-related protein |
CTRP5, MCOP5, NNO2, RD6 |
Curated: Gout, Microphthalmia, Microphthalmia with retinitis pigmentosa and ocular anomalies, Microphthalmos, Nanophthalmos, Optic atrophy, Retinitis pigmentosa
Unreviewed: N/A
|
715
|
|
|
Major facilitator superfamily domain containing 1 |
Minerva, SLC72A1, SMAP4 |
Curated: Obstructive pulmonary disease, Insomnia, Periodontitis
Unreviewed: Diabetes, Diabetes Mellitus, Hypertension, Obesity, Periodontosis
|
716
|
|
|
Major facilitator superfamily domain containing 11 |
ET |
Curated: N/A
Unreviewed: Asthma, Atherosclerosis, Atrial fibrillation, Breast neoplasm, Carcinogenesis, Chronic obstructive pulmonary disease, Colorectal neoplasm, Coronary artery disease, Coronary vasospasm, Endometrial neoplasm, Esophageal squamous cell carcinoma, Eye disease, Gestational diabetes, Heart failure, Hypertension, Hypertrophy, Hypoxia, Intracranial vasospasm, Nephrotic syndrome, Obesity, Ovarian neoplasm, Portal hypertension, Proximal symphalangism, Sarcoma, Sleep apnea, Squamous cell carcinoma, Thrombosis
|
717
|
|
|
Major facilitator superfamily domain containing 12 |
C19orf28, PP3501, SLC59B1 |
Curated: Crohn disease, Melanoma, Inflammatory bowel disease
Unreviewed: Malignant Neoplasm, Neoplasms, Neuroblastoma
|
718
|
|
|
MFSD12 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
719
|
|
|
Major facilitator superfamily domain containing 1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
720
|
|
|
MFSD2 lysolipid transporter A, lysophospholipid |
HsMFSD2A, MCPH15, MFSD2, NEDMISBA, NLS1, SLC59A1 |
Curated: Primary microcephaly, Hepatocellular carcinoma, Cryptorchidism, Febrile convulsion, Gross motor development delay, Intellectual developmental disorder, Metabolic syndrome, Microcephaly, Neurodevelopmental disorder, Diabetes mellitus type 2
Unreviewed: Agenesis Of Corpus Callosum, Alzheimer disease, Amyloidosis, Attention deficit hyperactivity disorder, Breast neoplasm, Cardiomegaly, Cerebellar Hypoplasia, Colitis, Congenital Clubfoot, Congenital Microcephaly, Dementia, Developmental Delay, Developmental disability, Dwarfism, Dyslalia, Gestational diabetes, Hepatitis b, Hyperlipidemia, Hypoplasia Of Corpus Callosum, Kawasaki disease, Lewy body disease, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Malignant Neoplasm, Mental retardation, Microlissencephaly, Multiple polyposis syndrome, Neoplasms, Neu-Laxova Syndrome, Neuronal Heterotopia, Obesity, Osteogenesis imperfecta, Pachygyria, Renal aplasia, Septicemia, Spastic tetraparesis, Speech Disorders, Stomach Carcinoma, Stomach Neoplasms, Ulcerative colitis, Vesicoureteral Reflux
|