Gene

CG43066

Species
Drosophila melanogaster
Symbol
CG43066
Name
Not Available
Synonyms
  • anon-WO0149848.1
  • CG42510
Biotype
protein coding gene
Automated Description
Predicted to enable L-amino acid transmembrane transporter activity; amino acid:sodium symporter activity; and neurotransmitter:sodium symporter activity. Predicted to be involved in glycine import across plasma membrane; neurotransmitter transport; and sodium ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including CNS glial cell; adult head; embryonic central brain neurons; embryonic head sensory system; and ganglia. Human ortholog(s) of this gene implicated in Hartnup disease and autosomal recessive intellectual developmental disorder 48. Orthologous to several human genes including SLC6A15 (solute carrier family 6 member 15) and SLC6A17 (solute carrier family 6 member 17).
FB Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11616
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

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
R6
Viewer Help
18.516M18.518M18.520M18.522M18.524M18.526M

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