Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
751 to 760 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

751
Myotrophin
GCDP, V-1
Bone disease, Cartilage disease, Dementia, Dry eye syndrome, Obesity, Periodontitis, Venous thromboembolism

752
MTR
5-methyltetrahydrofolate-homocysteine methyltransferase
HMAG, MS, cblG
Autism, Bipolar disorder, Breast neoplasm, Ischemic stroke, Cleft lip, Cleft palate, Complete unilateral cleft lip, Major depressive disorder, Digestive system disease, Disorders of intracellular cobalamin metabolism, Epilepsy, Gastrointestinal disease, Heart disease, Hematologic disease, Homocystinuria with megaloblastic anemia
View all (11 more)

753
Mitochondrial transcription rescue factor 1
C6orf203, HSPC230, PRED31
Prostate cancer, Hypertension

754
Mitochondrial translation release factor 1
MRF1, MTTRF1, RF1
Cardiovascular disease

755
Mitochondrial translation release factor in rescue
C12orf65, COXPD7, SPG55, mtRF-R
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
View all (4 more)

756
5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MSR, cblE
Anencephaly, Aprosencephaly, Ulcerative colitis, Colorectal neoplasm, Congenital septal defect of heart, Disorders of intracellular cobalamin metabolism, Heart disease, Homocystinuria with megaloblastic anemia, Hyperhomocysteinemia, Male infertility, Nervous system disease, Neural tube defect, Neural tube defects, folate-sensitive, Parkinson disease

757
MTSS I-BAR domain containing 1
MIM, MIMA, MIMB
Juvenile arthritis, Irritable bowel syndrome, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Peripheral arterial disease, Stomach neoplasms

758
MTSS I-BAR domain containing 2
ABBA, ABBA-1, ABBA1, IDDOF, MTSS1L
Alzheimer disease, Global developmental delay, Intellectual developmental disorder dysmorphic ocular, Intellectual developmental disorder

759
Microsomal triglyceride transfer protein
ABL, MTP
Abetalipoproteinemia, Autism, Celiac disease, Fatty liver, Fatty liver, alcoholic, Hypercholesterolemia, Hyperinsulinism, Hypertension, Liver disease, Nonalcoholic fatty liver disease, Obesity, Retinitis pigmentosa

760
Maturin, neural progenitor differentiation regulator homolog
C7orf41, Ells1
Dental caries