Gene

TMCO3

Species
Homo sapiens
Symbol
TMCO3
Name
transmembrane and coiled-coil domains 3
Synonyms
  • B230339H12Rik
  • C13orf11
Biotype
protein coding gene
Automated Description
Predicted to enable potassium:proton antiporter activity. Predicted to be involved in potassium ion transmembrane transport and proton transmembrane transport. Predicted to be located in membrane.
RGD Description
This gene encodes a member of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Members of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular membranes. Mutations in this gene have been identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract. [provided by RefSeq, Mar 2017]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR16254
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
GRCh38
Viewer Help
113.50M113.51M113.52M113.53M113.54M113.55M

Sequence Details

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Expression

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

Molecular Interactions

Genetic Interactions