Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (4) GO Terms (13) Nucleotides (322) Proteins (60) Interactants (447) Wiki
XB-GENEPAGE-951277
???displayGene.symbol???:
 hccs

???displayGene.name???: 
holocytochrome c synthase

???displayGene.synonyms???
cchl , hccs-a , hccs-b , mcops7 ( Nomenclature history )

???displayGene.geneFunction???
Holocytochrome c synthase/heme-lyase

AI Protein Function :
The hccs gene encodes holocytochrome c synthase, an enzyme localized to the mitochondrial inner membrane. This protein catalyzes the covalent attachment of heme to apocytochrome c, which is a required ...[+]


InterPro :
Cyt C/C1 haem lyase

???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
microphthalmia [+]

MIM:
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 1; LSDMCA1

External Links:
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info