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"
441 to 450 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

441
MKKS centrosomal shuttling protein
BBS6, HMCS, KMS, MKS
Alzheimer disease, Bardet-biedl syndrome, Congenital heart defects, Nephronophthisis, Obesity, Polycystic kidney disease, Cone dystrophy, Retinitis pigmentosa

442
Muskelin 1
TWA2
Alzheimer disease, Androgenetic alopecia, Asthma, Bipolar disorder, Central nervous system cancer, Melanoma, Dementia, Glioblastoma, Glioma, Lung cancer, Major depressive disorder, Pulmonary fibrosis, Schizophrenia, Urinary system disease

443
MAPK interacting serine/threonine kinase 1
MNK1
Kidney disease, Hypertension, Schizophrenia

444
MAPK interacting serine/threonine kinase 2
GPRK7, MNK2
Carpal tunnel syndrome

445
Makorin ring finger protein 1
RNF61
Alzheimer disease, Endometriosis

446
Makorin ring finger protein 2
HSPC070, RNF62
Gout, Leopard syndrome, Noonan syndrome

447
MKRN2 opposite strand
C3orf83, MKRN2-AS1
Hypertrophic cardiomyopathy, Systemic lupus erythematosus

448
Makorin ring finger protein 3
CPPB2, D15S9, RNF63, ZFP127, ZNF127
Central precocious puberty, Prader-willi syndrome, Scoliosis

449
MKS transition zone complex subunit 1
BBS13, JBTS28, MES, MKS, POC12
Bardet-biedl syndrome, Kidney disease, Ciliopathy, Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Leber congenital amaurosis, Meckel-gruber syndrome, Nystagmus, Optic atrophy, Peripheral neuropathy, Polycystic kidney disease, Polydactyly
View all (3 more)

450
Mohawk homeobox
C10orf48, IFRX, IRXL1
Alzheimer disease, Asthma, Carpal tunnel syndrome, Heart disease