Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7501 to 7510 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7501
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

7502
Matrix AAA peptidase interacting protein 1
C2orf47
Aortic disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Dilated cardiomyopathy, Insomnia, Metabolic syndrome, Schizophrenia, Substance abuse

7503
Membrane anchored junction protein
C11orf85
Hyperuricemia

7504
Male germ cell associated kinase
RP62
Alzheimer disease, Major depressive disorder, Mak-related retinopathy, Otosclerosis, Retinitis pigmentosa

7505
MAK16 homolog
MAK16L, RBM13
Intellectual developmental disorder

7506
Mal, T cell differentiation protein (MAL blood group)
HLD28, MVP17, VIP17
Breast neoplasms, Squamous cell carcinoma, Head and neck neoplasms, Hypomyelinating leukodystrophy, Metachromatic leukodystrophy, Pelizaeus-merzbacher disease

7507
MAM and LDL receptor class A domain containing 1
C10orf112, DIET1, bA265G8.2
Amblyopia, Ankylosing spondylitis, Color vision deficiency, Colorectal cancer, Coronary artery disease, Endometrial neoplasms, Gout, Henoch schoenlein purpura, Hyperuricemia, Lung cancer, Obesity, Obsessive-compulsive disorder

7508
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

7509
MAM domain containing 2
-
Carotid artery disease

7510
MAM domain containing 4
AEGP, EDTB
Schizophrenia