COX10 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	COX10
Gene name	cytochrome c oxidase assembly homolog 10 (yeast)
Chromosome	17
Chromosomal band	p12
Imprinted	Unknown
Genomic reference	NC_000017.10
Transcript reference	NM_001303.3
Associated with diseases	220110
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	69
Unique public DNA variants reported	64
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	2260
Entrez Gene	1352
PubMed articles	COX10
OMIM - Gene	602125
OMIM - Diseases	220110 (Mitochondrial complex IV deficiency, 220110 (3))
HGMD	COX10
GeneCards	COX10
GeneTests	COX10

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
00000076	17	COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast)	NM_001303.3	NP_001294.2	69

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