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"
641 to 650 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Mitochondrial ribosomal protein S22
C3orf5, COXPD5, GIBT, GK002, MRP-S22, ODG7, RPMS22, mS22
46, xx gonadal dysgenesis, Androgenetic alopecia, Breast neoplasms, Combined oxidative phosphorylation deficiency, Gonadal dysgenesis, Mitochondrial disease, Kawasaki disease, Obesity, Ovarian dysgenesis, Premature ovarian failure, Ovarian mucinous adenocarcinoma

642
Mitochondrial ribosomal protein S23
CGI-138, COXPD46, HSPC329, MRP-S23, mS23
Antiphospholipid syndrome, Breast neoplasms, Combined oxidative phosphorylation deficiency, Gout

643
Mitochondrial ribosomal protein S24
HSPC335, MRP-S24, S24mt, bMRP-47, bMRP47
Cataract

644
Mitochondrial ribosomal protein S25
COXPD50, MRP-S25, RPMS25, mS25
Combined oxidative phosphorylation deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy

645
Mitochondrial ribosomal protein S27
MRP-S27, S27mt, mS27
Central nervous system cancer, Glioblastoma, Glioma, Insomnia

646
Mitochondrial ribosomal protein S28
COXPD47, HSPC007, MRP-S28, MRP-S35, MRPS35
Breast neoplasms, Combined oxidative phosphorylation deficiency, Disorder of development or morphogenesis, Mitochondrial disease

647
Mitochondrial ribosomal protein S30
MRP-S30, PAP, PDCD9, S30mt, mL65
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Breast cancer, Kidney disease, Estrogen-receptor negative breast cancer, Lung cancer, Schizophrenia, Secondary malignant neoplasm, Squamous cell carcinoma, Substance abuse, Diabetes mellitus type 2

648
Mitochondrial ribosomal protein S31
IMOGN38, MRP-S31, S31mt, mS31
Myeloproliferative disorder

649
Mitochondrial ribosomal protein S33
CGI-139, MRP-S33, PTD003, S33mt, mS33
Bipolar disorder, Bipolar depression, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2

650
Mitochondrial ribosomal protein S34
COXPD32, MRP-S12, MRP-S34, MRPS12, mS34
Combined oxidative phosphorylation deficiency, Leigh syndrome, Mitochondrial disease