Aliases for C16orf89 Gene
External Ids for C16orf89 Gene
Previous GeneCards Identifiers for C16orf89 Gene
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]
GeneCards Summary for C16orf89 Gene
C16orf89 (Chromosome 16 Open Reading Frame 89) is a Protein Coding gene. Diseases associated with C16orf89 include Jackson-Weiss Syndrome. Gene Ontology (GO) annotations related to this gene include protein homodimerization activity.