Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "M"
671 to 680 of 898 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

671
MutS homolog 2
COCA1, FCC1, HNPCC, HNPCC1, LCFS2, LYNCH1, MMRCS2, MSH-2, hMSH2
Alzheimer disease, Lynch syndrome, Colorectal neoplasms, Congenital adrenal hyperplasia, Constitutional mismatch repair deficiency syndrome, Diverticular disease, Hereditary breast cancer, Hypertension, Pancreatic neoplasms, Constitutional mismatch repair deficiency, Muir-torre syndrome, Ovarian cancer, Ovarian cysts, Ovarian neoplasms, Prostate cancer
View all (3 more)

672
MutS homolog 3
DUP, FAP4, MRP1
Central nervous system cancer, Endometrial cancer, Endometrial neoplasms, Adenomatous polyposis, Glioblastoma, Glioma, Huntington disease, Lynch syndrome, Prostatic neoplasms, Rheumatic fever

673
MutS homolog 4
ASG, POF20, SPGF2
Gonadal dysgenesis, Premature ovarian failure, Spermatogenic failure, Testicular azoospermia

674
MutS homolog 5
G7, MUTSH5, NG23, POF13, SPGF74
Anxiety disorder, Autism, Azoospermia, Breast cancer, Hepatocellular carcinoma, Common variable immunodeficiency, Head and neck cancer, Hypothyroidism, Irritable bowel syndrome, Lung cancer, Major depressive disorder, Male infertility single gene azoospermia, Mastocytosis, Neurotic disorder, Non-small cell lung carcinoma
View all (11 more)

675
MutS homolog 6
GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3, MSH-6, p160
Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Color vision deficiency, Lynch syndrome, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Endometrial cancer, Endometrial neoplasms, Gaucher disease, Genetic predisposition to disease, Hereditary breast cancer, Hoarding disorder, Intellectual developmental disorder dysmorphic behavioral, Intracranial hemorrhage
View all (10 more)

676
Musashi RNA binding protein 1
-
Microcephaly, Rheumatoid arthritis

677
Musashi RNA binding protein 2
MSI2H
Androgenetic alopecia, Cannabis abuse, Clonal hematopoiesis, Color vision deficiency, Corneal neovascularization, Keratitis, Ovarian epithelial cancer, Metabolic syndrome, Open angle glaucoma, Ovarian cancer, Schizophrenia, Diabetes mellitus type 2

678
MSL complex subunit 1
MSL-1
Asthma, Central nervous system cancer, Glioblastoma, Glioma

679
MSL complex subunit 2
KBHS, MSL-2, MSL2L1, RNF184
Attention deficit hyperactivity disorder, Autism, Neurodevelopmental disorder, Coronary artery disease, Dementia, Myocardial infarction, Non-specific syndromic intellectual disability, Obesity, Schizophrenia, Diabetes mellitus type 2

680
MSL complex subunit 3
MRSXBA, MRXS36, MRXSBA, MSL3L1
Craniofacial abnormalities, Developmental disability, Global developmental delay, Intellectual developmental disorder