Gene

hccsb

ID
ZDB-GENE-000607-78
Name
holocytochrome c synthase b
Symbol
hccsb Nomenclature History
Previous Names
  • hccs
  • id:ibd1278 (1)
  • wu:fb18h01 (1)
  • wu:fc64e12 (1)
  • wu:fi43e01 (1)
Type
protein_coding_gene
Location
Chr: 24 Mapping Details/Browsers
Description
Predicted to have holocytochrome-c synthase activity. Predicted to be involved in cytochrome c-heme linkage. Predicted to localize to mitochondrion. Human ortholog(s) of this gene implicated in microphthalmia. Is expressed in several structures, including adaxial cell; alar plate midbrain region; immature eye; musculature system; and retina. Orthologous to human HCCS (holocytochrome c synthase).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
8 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With hccsb Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
linear skin defects with multiple congenital anomalies 1 Alliance Linear skin defects with multiple congenital anomalies 1 309801
Associated With hccsb Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR000511 Holocytochrome c/c1 synthase
Domain Details Per Protein
Protein Length Holocytochrome c/c1 synthase
UniProtKB:Q803H2 269
UniProtKB:A0A0R4IKC6 47
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations