Gene

slc22a5

Species
Danio rerio
Symbol
slc22a5
Name
solute carrier family 22 member 5
Synonyms
  • octn2
  • si:ch211-25g7.3
Biotype
protein coding gene
Automated Description
Enables carnitine transmembrane transporter activity. Acts upstream of or within carnitine transport and heme biosynthetic process. Predicted to be located in apical plasma membrane. Is expressed in several structures, including gill; head; liver; pleuroperitoneal region; and skeletal muscle. Human ortholog(s) of this gene implicated in Crohn's disease; cardiomyopathy; inherited metabolic disorder; and systemic primary carnitine deficiency disease. Orthologous to human SLC22A5 (solute carrier family 22 member 5).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24064
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
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
GRCz11
Viewer Help
45.660M45.662M45.664M45.666M45.668M45.670M

Sequence Details

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Expression

Primary Sources
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions