Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
211 to 220 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
Membrane bound transcription factor peptidase, site 2
BRESEK, IFAP, KFSD, KFSDX, OI19, OLMSX, S2P
Bone fragility with contractures, arterial rupture, and deafness, Brain anomalies ectodermal dysplasia skeletal malformations hirschsprung disease syndrome, Bresek syndrome, Hepatocellular carcinoma, Congenital palmoplantar and perioral keratoderma of olmsted, Desbuquois syndrome, Keratosis follicularis spinulosa decalvans, Keratosis follicularis spinulosa decalvans, x-linked, Olmsted syndrome, x-linked, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

212
Melanocortin 1 receptor
CMM5, MSH-R, SHEP2
Basal cell carcinoma, Blepharitis, Melanoma, Cutaneous squamous cell carcinoma, Major depressive disorder, Erythematosquamous dermatosis, Hyperalgesia, Keratinocyte carcinoma, Non-melanoma skin carcinoma, Non-small cell lung carcinoma, Oculocutaneous albinism, Respiratory system neoplasm, Rosacea, Sebaceous gland disease, Seborrheic dermatitis
View all (5 more)

213
Melanocortin 2 receptor
ACTHR
Bipolar disorder, Ciliopathy, Cryptogenic west syndrome, Eye disease, Glucocorticoid deficiency, Hypertension, Anterior segment dysgenesis, Prostatic neoplasms, Infantile spasms, West syndrome

214
Melanocortin 3 receptor
BMIQ9, MC3, MC3-R, OB20, OQTL
Alzheimer disease, Body mass index, Dementia, Obesity

215
Melanocortin 4 receptor
BMIQ20
Anhedonia, Atrial fibrillation, Body mass index, Body weight, Breast cancer, Cardiovascular disease, Lymphocytic leukemia, Coronary artery disease, Dental caries, Major depressive disorder, Gallstones, Gout, Hyperinsulinism, Hypertension, Diabetes mellitus type 2
View all (8 more)

216
Melanocortin 5 receptor
MC2
Kidney disease, Ciliopathy, Color vision deficiency, Eye disease, Anterior segment dysgenesis, Kidney failure, Major depressive disorder, Schizophrenia

217
Melanoma cell adhesion molecule
CD146, HEMCAM, METCAM, MUC18, MelCAM
Autoimmune nervous system disorder, Mesothelioma, Multiple sclerosis, Peritoneal neoplasms

218
Malonyl-CoA-acyl carrier protein transacylase
FASN2C, MCT, MCT1, MT, NET62, OPA15, fabD
Optic atrophy, Schizophrenia

219
MCC regulator of Wnt signaling pathway
MCC1
Autism, Bipolar disorder, Cerebral amyloid angiopathy, Color vision deficiency, Colorectal cancer, Colorectal neoplasms, Hypertension, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

220
Methylcrotonyl-CoA carboxylase subunit 1
MCC-B, MCCA, MCCCalpha
3-methylcrotonyl-coa carboxylase deficiency, Lewy body disease, Parkinson disease, Prostate cancer