The MRPS16 gene homepage

General information
Gene symbol MRPS16
Gene name mitochondrial ribosomal protein S16
Chromosome 10
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NG_008096.1
Transcript reference NM_016065.3
Exon/intron information NM_016065.3 exon/intron table
Associated with diseases COXPD-2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 5
Unique public DNA variants reported 5
Individuals with public variants 1
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated September 15, 2020
Version MRPS16:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_016065.3.
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
Homepage URL https://www.LOVD.nl/MRPS16
HGNC 14048
Entrez Gene 51021
PubMed articles MRPS16
OMIM - Gene 609204
OMIM - Diseases COXPD-2 (combined oxidative phosphorylation deficiency, type 2 (COXPD-2))
HGMD MRPS16
GeneCards MRPS16
GeneTests MRPS16
Orphanet MRPS16


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00013902 10 mitochondrial ribosomal protein S16 NM_016065.3 NP_057149.1 5


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