Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
891 to 898 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

891
Myosin VIIA and Rab interacting protein
SLAC2-C, SLAC2C
Alzheimer disease, Lymphoblastic leukemia, Connective tissue disease, Male reproductive system disease, Mixed connective tissue disease, Pulmonary edema

892
Myb like, SWIRM and MPN domains 1
2A-DUB, 2ADUB, BMFS4
Aortic stenosis, Aortic valve disease, Bone marrow failure syndromes, Congenital progressive bone marrow failure-b-cell immunodeficiency-skeletal dysplasia syndrome, Diabetic retinopathy, Willis-ekbom disease

893
Myelin transcription factor 1
C20orf36, MTF1, MYTI, NZF2, PLPB1, ZC2H2C1, ZC2HC4A
Asthma, Autism, Bell's palsy, Breast cancer, Cervical cancer, Craniofacial microsomia, Diverticular disease, Goldenhar syndrome, Intellectual developmental disorder, Movement disorder, Periodic limb movement disorder, Willis-ekbom disease, Schizoaffective disorder, Hereditary spastic paraplegia, Diabetes mellitus, type 2

894
Myelin transcription factor 1 like
MRD39, NZF1, ZC2H2C2, ZC2HC4B, myT1-L
Eczema, Attention deficit hyperactivity disorder, Autism, Color vision deficiency, Diabetic retinopathy, Iga nephropathy, Inflammatory skin disease, Insomnia, Intellectual developmental disorder, Major depressive disorder, Colorectal adenoma, Mood disorder, Neurodevelopmental disorder, Neurotic disorder, Psoriasis
View all (6 more)

895
Myocardial zonula adherens protein
CMD2K, GCOM1, Gup, MYOZAP
Juvenile arthritis, Astrocytoma, Atrial fibrillation, Dilated cardiomyopathy, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Substance abuse

896
Myeloid zinc finger 1
MZF-1, MZF1B, ZFP98, ZNF42, ZSCAN6
Colorectal adenoma, Colorectal cancer

897
Mitotic spindle organizing protein 2A
FAM128A, MOZART2A
Keratoconus

898
Mitotic spindle organizing protein 2B
FAM128B, MOZART2B
Congenital microcephaly, Global developmental delay, Lissencephaly, Neurodevelopmental disorder