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"
41 to 50 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
MAGE family member E1
DAMAGE, HCA1
Bile duct disease, Liver cirrhosis

42
MAGE family member E2
HCA3
Male infertility single gene azoospermia

43
MAGE family member F1
MAGE-F1
Androgenetic alopecia, Color vision deficiency, Glomerulonephritis, Oligodendroglioma, Prostate cancer

44
MAGE family member H1
APR-1, APR1, MAGEH
Androgenetic alopecia

45
MAGE family member L2
NDNL1, PWLS, SHFYNG, nM15
Ambiguous genitalia, Autism, Contracture of multiple joints, Developmental disability, Fetal akinesia deformation sequence, Intellectual developmental disorder, Neurodevelopmental disorder, Pena-shokeir syndrome , Prader-willi syndrome, Psychiatric disorders, Schaaf-yang syndrome, Scoliosis

46
Membrane associated guanylate kinase, WW and PDZ domain containing 1
AIP-3, AIP3, BAIAP1, BAP-1, BAP1, MAGI-1, MAGI-1b, Magi1d, TNRC19, WWP3
Asthma, Bipolar disorder, Adenoid cystic carcinoma, Central nervous system cancer, Corneal astigmatism, Crohn disease, Glioblastoma, Glioma, Ileocolitis, Insomnia, Major depressive disorder, Neurotic disorder, Ocular sarcoidosis, Osteoarthritis, Prostate cancer
View all (2 more)

47
Membrane associated guanylate kinase, WW and PDZ domain containing 2
ACVRIP1, AIP-1, AIP1, ARIP1, MAGI-2, NPHS15, SSCAM
Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Bronchopulmonary dysplasia, Cannabis abuse, Adenoid cystic carcinoma, Central nervous system cancer, Cervical cancer, Lymphoblastic leukemia, Colorectal cancer, Developmental and epileptic encephalopathy, Epilepsy, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Glioblastoma
View all (17 more)

48
Membrane associated guanylate kinase, WW and PDZ domain containing 3
MAGI-3, dJ730K3.2
Arthrogryposis multiplex congenita, Autoimmune thyroid disease, Breast cancer, Bulimia, Coronary artery disease, Crohn disease, Melanoma, Heart failure, Hodgkin lymphoma, Hypothyroidism, Immune system disease, Inflammatory bowel disease, Leprosy, Lung cancer, Myasthenia gravis
View all (8 more)

49
Mago homolog B, exon junction complex subunit
MGN2, mago, magoh
Ovarian cysts

50
Magnesium transporter 1
CDG1CC, IAP, MRX95, OST3B, PRO0756, SLC58A1, XMEN, bA217H1.1
Congenital disorder of glycosylation, Developmental disability, Graves disease, Intellectual developmental disorder, x-linked, X-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia, X-linked intellectual disability, X-linked immunodeficiency with magnesium defect