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"
801 to 810 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
Myosin binding protein H like
-
Attention deficit hyperactivity disorder, Autism, Brugada syndrome, Dilated cardiomyopathy, Non-immune hydrops fetalis, Hypertrophic cardiomyopathy

802
MYC proto-oncogene, bHLH transcription factor
MRTL, MYCC, bHLHe39, c-Myc
Asthma, Burkitt lymphoma, Carcinoma, Ductal carcinoma, Hepatocellular carcinoma, Merkel cell carcinoma, Non-small-cell lung carcinoma, Squamous cell carcinoma, Cardiomyopathy, Cleft lip, Cleft palate, Colonic neoplasms, Colorectal neoplasms, Complete unilateral cleft lip, Demyelinating diseases
View all (25 more)

803
MYC binding protein
AMY-1
Alzheimer disease, Adenoid cystic carcinoma

804
MYC binding protein 2
Myc-bp2, PAM, PHR1, Phr
Gastric cancer, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Preeclampsia

805
MYCBP associated protein
AMAP-1, AMAP1
Spermatogenic failure

806
MYCL proto-oncogene, bHLH transcription factor
L-Myc, LMYC, MYCL1, bHLHe38
Medulloblastoma, Metabolic syndrome, Prostatic neoplasms, Small cell lung carcinoma, Diabetes mellitus type 2

807
MYCN proto-oncogene, bHLH transcription factor
FGLDS1, MODED, MPAPA, MYCNsORF, MYCNsPEP, N-myc, NMYC, ODED, bHLHe37
Adenoid cystic carcinoma, Basal cell carcinoma, Desbuquois syndrome, Double outlet right ventricle, Feingold syndrome, Gallbladder agenesis, Hyperplasia, Medulloblastoma, Necrosis, Neuroblastoma, Ventricular septal defect, Wilms tumor

808
MYC target 1
MTLC
Uterine fibroid

809
MYD88 innate immune signal transduction adaptor
IMD68, MYD88D, WM1
Cholelithiasis, Depression, Eosinophilia, Hypertension, Immunodeficiency, Lymphoma, Diffuse large b-cell lymphoma, Waldenstrom macroglobulinemia

810
Myeloid derived growth factor
C19orf10, EUROIMAGE1875335, IL25, IL27, IL27w, R33729_1, SF20
Alzheimer disease