POLG2 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	POLG2
Gene name	polymerase (DNA directed), gamma 2, accessory subunit
Chromosome	17
Chromosomal band	q23.3
Imprinted	Unknown
Genomic reference	NC_000017.10
Transcript reference	NM_007215.3
Associated with diseases	610131
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	27
Unique public DNA variants reported	20
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	9180
Entrez Gene	11232
PubMed articles	POLG2
OMIM - Gene	604983
OMIM - Diseases	610131 (Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, 610131 (3))
HGMD	POLG2
GeneCards	POLG2
GeneTests	POLG2

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
00000268	17	polymerase (DNA directed), gamma 2, accessory subunit	NM_007215.3	NP_009146.2	27

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