Mitochondrial ribosomal protein s22

Preferred Label : Mitochondrial ribosomal protein s22;

Symbol : MRPS22;

CISMeF acronym : MRPS22;

Type : Gene;

Alternative titles and symbols : Chromosome 3 open reading frame 5; C3ORF5;

Ensembl ID : ENSG00000175110;

Prefixed ID : *605810;

Details

Origin ID

605810;

UMLS CUI

C1422713;

Automatic exact mappings (from CISMeF team)
- MRPS22 gene [LOINC component]
- mitochondrial ribosomal protein S22 [ORDO Gene]
- mitochondrial ribosomal protein S22 [HGNC gene]
HGNC gene
- mitochondrial ribosomal protein S22 [HGNC gene]
ORDO concept(s)
- mitochondrial ribosomal protein S22 [ORDO Gene]
Phenotypes related
- Combined oxidative phosphorylation deficiency 5 [OMIM Phenotype]
- Ovarian dysgenesis 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MRPS22 gene [LOINC component]
- mitochondrial ribosomal protein S22 [HGNC gene]

Keyword's position in hierarchy(ies) :

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