7491
|
|
|
MAGE family member D4B |
- |
|
7492
|
|
|
MAGE family member E1 |
DAMAGE, HCA1 |
|
7493
|
|
|
MAGE family member E2 |
HCA3 |
|
7494
|
|
|
MAGE family member F1 |
MAGE-F1 |
|
7495
|
|
|
MAGE family member H1 |
APR-1, APR1, MAGEH |
|
7496
|
|
|
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 |
7497
|
|
|
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, Schizophrenia, ScoliosisView all (2 more) |
7498
|
|
|
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, Glioma, Hereditary steroid-resistant nephrotic syndrome, Hypertrophic cardiomyopathy, Insomnia, Major depressive disorder, Memory disorders, Metabolic syndrome, Moyamoya disease, Nephrotic syndrome, Non-small cell lung carcinoma, Obesity, Oligodendroglioma, Schizophrenia, Substance abuse, Diabetes mellitus type 2, Urethral syndrome, Visual disorderView all (17 more) |
7499
|
|
|
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, Lung cancer, Myasthenia gravis, Myocardial infarction, Neuroblastoma, Pena-shokeir syndrome , Rheumatoid arthritis, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2View all (7 more) |
7500
|
|
|
Mago homolog B, exon junction complex subunit |
MGN2, mago, magoh |
|
