Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7641 to 7650 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7641
MYC associated factor X
PDMCS, bHLHd4
Osteoarthritis, Pheochromocytoma, Polydactyly-macrocephaly syndrome, Wilms tumor

7642
MYC associated zinc finger protein
PUR1, Pur-1, SAF-1, SAF-2, SAF-3, ZF87, ZNF801, Zif87
Multiple sclerosis

7643
Mab-21 domain containing 2
C3orf59, D2A, hMB21D2
Alzheimer disease, Autoimmune disease, Hypothyroidism, Rheumatoid arthritis

7644
Methyl-CpG binding domain protein 1
CXXC3, PCM1, RFT
Prostatic neoplasms

7645
Methyl-CpG binding domain protein 2
DMTase, NY-CO-41
Benign prostatic hyperplasia, Bipolar disorder, Corneal edema, Hoarding disorder, Inflammatory bowel disease, Lung cancer, Neurotic disorder, Oligodendroglioma, Periodontitis, Prostate cancer, Prostatic neoplasms, Psoriasis, Psoriasis vulgaris, Schizophrenia

7646
Methyl-CpG binding domain protein 3
-
Alzheimer disease, Autism

7647
Methyl-CpG binding domain protein 3 like 2
-
Stomach neoplasms

7648
Methyl-CpG binding domain 4, DNA glycosylase
MED1, TPDS2, UVM1
Systemic scleroderma, Autism, Rheumatoid arthritis, Tumor predisposition syndrome, Uveal melanoma

7649
Methyl-CpG binding domain protein 5
C2DELq23.1, DEL2Q23.1, MRD1
Atrial fibrillation, Autism, Nonsyndromic intellectual disability, Bipolar disorder, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Global developmental delay, Gout, Intellectual developmental disorder, Major depressive disorder, Myocardial infarction, Neurotic disorder, Non-specific syndromic intellectual disability, Peripheral arterial disease, Schizophrenia

7650
Methyl-CpG binding domain protein 6
-
Autism