help  | about  | cite  | software

Gene : HCCS Homo sapiens

Name  ? holocytochrome c synthase Cytological Location  Xp22.2
Brief Description  holocytochrome c synthase
description  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]
  • synonyms:
  • microphthalamia with linear skin defects,
  • MLS,
  • holocytochrome c synthase (cytochrome c heme-lyase),
  • MLS,
  • LSDMCA1,
  • NM_001122608,
  • uc004cuj.4,
  • CCHL,
  • HGNC:4837,
  • HCCS,
  • CCHL,
  • cytochrome c heme-lyase,
  • MCOPS7,
  • OTTHUMG00000021128
  • identifiers:
  • 3052,
  • ENSG00000004961,
  • HCCS

Genome feature

Region: gene ? Length: 11755  
Location: X:11111332-11123086 Cyto location: Xp22.2

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer

Gene --> Orthologues


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



384 SN Ps

5 Cross References

19 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results