|
881
|
|
|
Membrane frizzled-related protein |
CTRP5, MCOP5, NNO2, RD6 |
Disorder of eye, Glaucoma, Hyperopia, Retinal degeneration, Microphthalmia, with retinitis pigmentosa, foveoschisis, and optic disc drusen, Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome, Microphthalmos, Nanophthalmos, Nyctalopia, Optic disk drusen, Retinal dystrophy, Rod-cone dystrophy, Strabismus |
|
882
|
|
|
Mitotic arrest deficient 1 like 1 |
MAD1, MVA7, PIG9, TP53I9, TXBP181 |
Arthritis, Bipolar disorder, Cardiovascular diseases, Coronary artery disease, Depressed bipolar disorder, Development disorder, Gastroesophageal reflux disease, Juvenile arthritis, Lymphoma, Mental disorders, Mental depression, Mood disorder, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Psychosis, Schizoaffective disorder, Schizophrenia, Somatic lymphoma, Still disease, Testicular neoplasms, Testicular germ cell tumorView all (10 more) |
|
883
|
|
|
Maestro |
B29, C18orf3 |
|
|
884
|
|
|
Magnesium transporter 1 |
CDG1CC, IAP, MRX95, OST3B, PRO0756, SLC58A1, XMEN, bA217H1.1 |
|
|
885
|
|
|
MINDY lysine 48 deubiquitinase 4 |
AQP-1, AQP1, C7orf67, CHIP28, FAM188B |
|
|
886
|
|
|
Migration and invasion enhancer 1 |
C17orf37, C35, ORB3, RDX12, XTP4 |
|
|
887
|
|
|
MON1 vesicular trafficking associated A |
SAND1 |
|
|
888
|
|
|
Mastermind like transcriptional coactivator 2 |
MAM-3, MAM2, MAM3, MLL-MAML2 |
Arthritis, Central nervous system neoplasms, Glioma, Inflammatory bowel disease, Juvenile arthritis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Schizophrenia, Still disease, Ulcerative colitis |
|
889
|
|
|
Multiple EGF like domains 10 |
CMYO10A, CMYO10B, CMYP10A, CMYP10B, EMARDD, SR-F3 |
Alzheimer disease, Congenital alveolar dysplasia, Congenital clubfoot, Congenital pectus excavatum, Dysphagia, Esophageal dysphagia, Facial paralysis, High palate, Motor delay, Myopathy, Myopathy, areflexia, respiratory distress, and dysphagia, Myopathy-areflexia-respiratory distress-dysphagia syndrome, Hypotonia, Oropharyngeal dysphagia, Respiratory failure, Schizophrenia, ScoliosisView all (2 more) |
|
890
|
|
|
Minichromosome maintenance 8 homologous recombination repair factor |
C20orf154, POF10, dJ967N21.5 |
|
