Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
121 to 130 of 971 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

121
MALT1 paracaspase
IMD12, MLT, MLT1, PCASP1
Color vision deficiency, Combined immunodeficiency disease, Immunodeficiency, Diffuse large b-cell lymphoma, Malt lymphoma, Multiple sclerosis, Neuroblastoma, Severe combined immunodeficiency

122
Myotubularin related protein 11
CRA
Androgenetic alopecia, Breast cancer, Carpal tunnel syndrome, Obstructive pulmonary disease, Open angle glaucoma, Scoliosis

123
MAGE family member D2
11B6, BARTS5, BCG-1, BCG1, HCA10, MAGE-D2
Bartter syndrome, Attention deficit hyperactivity disorder, Cerebellar atrophy, Dandy-walker syndrome, Global developmental delay, Neurotic disorder

124
Mortality factor 4 like 1
Eaf3, FWP006, HsT17725, MEAF3, MORFRG15, MRG15, S863-6
Adenoid cystic carcinoma, Cardiovascular disease, Coronary artery disease, Heart disease, Lung cancer, Major depressive disorder, Multiple sclerosis, Myocardial infarction, Myocardial ischemia, Nephrotic syndrome, Squamous cell carcinoma, Diabetes mellitus, type 2

125
MSL complex subunit 3
MRSXBA, MRXS36, MRXSBA, MSL3L1
Craniofacial abnormalities, Developmental disability, Global developmental delay, Intellectual developmental disorder

126
Microtubule associated protein RP/EB family member 2
CSCSC2, EB1, EB2, RP1
Brugada syndrome, Central nervous system cancer, Color vision deficiency, Developmental disability, Glioma, Hypertrophic cardiomyopathy, Scoliosis

127
MiR-302/367 cluster host gene
-

128
Methionyl aminopeptidase 2
MAP2, MNPEP, p67eIF2

129
MIR4527 host gene
-

130
Midline 2
FXY2, MRX101, RNF60, TRIM1, XLID101
Esophageal atresia, Intellectual developmental disorder, x-linked, X-linked intellectual disability