Gene

C16orf89

Species
Homo sapiens
Symbol
C16orf89
Name
chromosome 16 open reading frame 89
Synonyms
  • hypothetical protein LOC146556
  • MGC45438
Biotype
protein coding gene
Automated Description
Enables protein homodimerization activity. Located in cytosol and membrane.
RGD Description
This gene is expressed predominantly in the thyroid. Based on expression patterns similar to thyroid transcription factors and proteins, this gene may function in the development and function of the thyroid. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR33539
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
5.044M5.046M5.048M5.050M5.052M5.054M5.056M5.058M5.060M5.062M5.064M5.066M

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