Gene

hccs.L

Species
Xenopus laevis
Symbol
hccs.L
Name
holocytochrome c synthase
Synonyms
  • cchl
  • hccs-a
Biotype
gene
Automated Description
Predicted to enable holocytochrome-c synthase activity and metal ion binding activity. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in linear skin defects with multiple congenital anomalies 1 and microphthalmia. Orthologous to human HCCS (holocytochrome c synthase).
XBXL Description
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
XL9.2
Viewer Help
92.3695M92.3700M92.3705M92.3710M92.3715M92.3720M92.3725M92.3730M92.3735M92.3740M92.3745M

Sequence Details

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Expression

Primary Sources
Other Sources
None
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions