holocytochrome c synthase

Summary
Gene Symbol
  • HCCS
Organism
Homo sapiens (human)
NCBI Gene
3052
PubChem
3052
Alliance of Genome Resources
Annotation
Keyword
  • Disease variant
  • Heme
  • Lyase
  • Microphthalmia
  • Mitochondrion inner membrane
  • Myristate
  • Reference proteome
  • Repeat
Proteins
Displaying 1 entry
UniProt Protein Name
P53701
  • Cytochrome c-type heme lyase
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
cytochrome c heme lyase
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Displaying 1 entry
InterPro
Holocytochrome c/c1 synthase
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0111808 linear skin defects with multiple congenital anomalies 1
DOID:10629 microphthalmia

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024