View MRPS16 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol MRPS16
Gene name mitochondrial ribosomal protein S16
Chromosome 10
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NC_000010.10
Transcript reference NM_016065.3
Associated with diseases COXPD2
Citation reference(s) -
Curators (0) -
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 0
Hidden variants 0
Notes MSeqDR-LSDB
Date created November 07, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 14048
Entrez Gene 51021
PubMed articles MRPS16
OMIM - Gene 609204
OMIM - Diseases COXPD2 (Combined oxidative phosphorylation deficiency 2, 610498 (3))
HGMD MRPS16
GeneCards MRPS16
GeneTests MRPS16


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000175 10 mitochondrial ribosomal protein S16 NM_016065.3 NP_057149.1 1


Copyright & disclaimer
Sources: GeneDX http://www.genedx.com ; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium