HCCS

GENE INFORMATION

? »

Gene name

HCCS (HGNC Symbol)

Synonyms

CCHL

Description

holocytochrome c synthase (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]

Chromosome

X (Chromosome progress)

Cytoband

p22.2

Chromosome location (bp)

11129421 - 11141198

Ensembl

ENSG00000004961 (version 73.37)

Entrez gene

3052

UniProt

P53701 (UniProt - Evidence at protein level)

neXtProt

NX_P53701

Antibodypedia

HCCS antibodies
 

PROTEIN VIEW

? »
 
 
 
HCCS-001
 
HCCS-002
 
HCCS-003
 
 
 
 
 

PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HCCS-001 ENSP00000326579
ENST00000321143
P53701
Show all »
Show » Show » 268 30.6 Yes 0
HCCS-002 ENSP00000370139
ENST00000380762
P53701
Show all »
Show » Show » 268 30.6 Yes 0
HCCS-003 ENSP00000370140
ENST00000380763
P53701
Show all »
Show » Show » 268 30.6 Yes 0