HCCS gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol HCCS
Gene name holocytochrome c synthase
Chromosome X
Chromosomal band p22
Imprinted Unknown
Genomic reference NC_000023.10
Transcript reference NM_001122608.2, NM_001171991.2, NM_005333.4
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Notes MSeqDR-LSDB
Date created November 12, 2013
Links to other resources
HGNC 4837
Entrez Gene 3052
PubMed articles HCCS
OMIM - Gene 300056
HGMD HCCS
GeneCards HCCS
GeneTests HCCS


Active transcripts


ID     
Chr     
Name     
NCBI ID     
NCBI Protein ID     
DescendingVariants     
00000792 X transcript variant 1 NM_005333.4 NP_005324.3 0
00000793 X transcript variant 2 NM_001122608.2 NP_001116080.1 0
00000794 X transcript variant 3 NM_001171991.2 NP_001165462.1 0


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; NuclearMitome http://www.transgenomic.com ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

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