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, LS
Citation reference(s) -
Curators (0) -
Total number of public variants reported 65
Unique public DNA variants reported 60
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))
LS (Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3))
HGMD COX10
GeneCards COX10
GeneTests COX10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000076 17 COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast) NM_001303.3 NP_001294.2 65


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