MRPS2 (mitochondrial ribosomal protein S2)

2014-11-01  

Identity

HGNC
LOCATION
9q34.3
LOCUSID
ALIAS
CGI-91,COXPD36,MRP-S2,S2mt
FUSION GENES

Other Information

Locus ID:

NCBI: 51116
MIM: 611971
HGNC: 14495
Ensembl: ENSG00000122140

Variants:

dbSNP: 51116
ClinVar: 51116
TCGA: ENSG00000122140
COSMIC: MRPS2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000122140ENST00000241600Q9Y399
ENSG00000122140ENST00000371785Q9Y399
ENSG00000122140ENST00000453385Q5T8A0

Expression (GTEx)

0
10
20
30
40
50
60

Pathways

PathwaySourceExternal ID
RibosomeKEGGko03010
RibosomeKEGGhsa03010
Organelle biogenesis and maintenanceREACTOMER-HSA-1852241
Mitochondrial translationREACTOMER-HSA-5368287
Mitochondrial translation initiationREACTOMER-HSA-5368286
Mitochondrial translation elongationREACTOMER-HSA-5389840
Mitochondrial translation terminationREACTOMER-HSA-5419276

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
295762192018Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.32
295762192018Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.32
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20

Citation

Dessen P

MRPS2 (mitochondrial ribosomal protein S2)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/70478/js/lib/teaching-explorer/