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MGP005098

UniProt Annotations

Entry Information
Gene Namemitochondrial ribosomal protein S16
Protein EntryRT16_HUMAN
UniProt IDQ9Y3D3
SpeciesHuman
Comments
Comment typeDescription
Alternative ProductsEvent=Alternative splicing; Named isoforms=2; Name=1; IsoId=Q9Y3D3-1; Sequence=Displayed; Name=2; IsoId=Q9Y3D3-2; Sequence=VSP_056498; Note=No experimental confirmation available.;
DiseaseCombined oxidative phosphorylation deficiency 2 (COXPD2) [MIM:610498]: A mitochondrial disease resulting in fatal neonatal metabolic acidosis with agenesis of the corpus callosum. {ECO:0000269|PubMed:15505824}. Note=The disease is caused by mutations affecting the gene represented in this entry.
SimilarityBelongs to the ribosomal protein S16P family. {ECO:0000305}.
Subcellular LocationMitochondrion.
SubunitComponent of the mitochondrial ribosome small subunit (28S) which comprises a 12S rRNA and about 30 distinct proteins.
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