The HCCS gene homepage

General information
Gene symbol HCCS
Gene name holocytochrome c synthase
Chromosome X
Chromosomal band p22
Imprinted Unknown
Genomic reference NG_016460.1
Transcript reference NM_001122608.2, NM_001171991.2, NM_005333.4
Associated with diseases ID, MCOPS-7
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 3
Date created November 30, -0001

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:4837
Entrez Gene 3052
PubMed articles HCCS
OMIM - Gene 300056
OMIM - Diseases MCOPS-7 (microphthalmia syndromic, type 7 (MCOPS-7))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00028474 X transcript variant 1 NM_005333.4 NP_005324.3 -
00028475 X transcript variant 2 NM_001122608.2 NP_001116080.1 -
00028476 X transcript variant 3 NM_001171991.2 NP_001165462.1 -