Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
181 to 190 of 971 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

181
MDS1 and EVI1 complex locus
AML1-EVI-1, EVI1, KMT8E, MDS1, MDS1-EVI1, PRDM3, RUSAT2
Alzheimer disease, Aortic stenosis, Aortic valve disease, Asthma, Biliary tract cancer, Breast cancer, Breast neoplasm, Cancer, Cardiovascular disease, Cervical cancer, Obstructive pulmonary disease, Colonic neoplasm, Colorectal cancer, Coronary artery disease, Desbuquois syndrome
View all (39 more)

182
Membrane spanning 4-domains A2
APY, ATOPY, FCER1B, FCERI, IGEL, IGER, IGHER
Alzheimer disease, Asthma, Atopic dermatitis, Hypersensitivity, Rhinitis

183
Membrane associated ring-CH-type finger 8
CMIR, MARCH-VIII, MARCH8, MIR, RNF178, c-MIR
Cholecystolithiasis, Esophageal neoplasm, Gallstones, Prostate cancer

184
Mitogen-activated protein kinase 15
ERK7, ERK8
Obesity, Urinary bladder cancer

185
Muscle RAS oncogene homolog
M-RAs, NS11, R-RAS3, RRAS3
Attention deficit hyperactivity disorder, Cardiovascular disease, Carotid artery disease, Ischemic heart disease, Coronary artery disease, Desbuquois syndrome, Diabetes mellitus type 2, Dyslexia, Hypertension, Gout, Male infertility single gene azoospermia, Metabolic syndrome, Myocardial infarction, Myocardial ischemia, Noonan syndrome
View all (3 more)

186
MLX interacting protein
MIR, MONDOA, bHLHe36
Eczema, Gout, Inflammatory skin disease, Osteoarthritis, Psoriasis, Schizophrenia

187
MORC family CW-type zinc finger 2
CMT2Z, DIGFAN, ZCW3, ZCWCC1
Charcot-marie-tooth disease, Distal hereditary motor neuropathy, Developmental delay with impaired growth and dysmorphic facies, Distal spinal muscular atrophy, Global developmental delay, Leigh syndrome, Neurodevelopmental disorders

188
Multimerin 1
ECM, EMILIN4, GPIa*, MMRN
Insomnia, Irritable bowel syndrome, Large artery stroke, Male infertility single gene azoospermia, Neurotic disorder, Parkinson disease

189
Microtubule associated protein RP/EB family member 1
EB1
Attention deficit hyperactivity disorder, Myocardial ischemia, Polycystic ovary syndrome, Prostate cancer

190
Microtubule associated protein RP/EB family member 3
EB3, EBF3, EBF3-S, RP3
Anxiety disorder, Polycystic ovary syndrome, Diabetes mellitus, type 2