MRPS22 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	MRPS22
Gene name	mitochondrial ribosomal protein S22
Chromosome	3
Chromosomal band	q23
Imprinted	Unknown
Genomic reference	NC_000003.11
Transcript reference	NM_020191.2
Associated with diseases	COXPD5
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	18
Unique public DNA variants reported	16
Individuals with public variants	0
Hidden variants	0
Download all this gene's data	Download all data
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	14508
Entrez Gene	56945
PubMed articles	MRPS22
OMIM - Gene	605810
OMIM - Diseases	COXPD5 (Combined oxidative phosphorylation deficiency 5, 611719 (3))
HGMD	MRPS22
GeneCards	MRPS22
GeneTests	MRPS22

Active transcripts

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00000176	3	mitochondrial ribosomal protein S22	NM_020191.2	NP_064576.1	18

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

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium