Homo sapiens Gene: C16orf89
Summary
InnateDB Gene IDBG-13441.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C16orf89
Gene Name chromosome 16 open reading frame 89
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000153446
Encoded Proteins
chromosome 16 open reading frame 89
chromosome 16 open reading frame 89
chromosome 16 open reading frame 89
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:5044122-5066110
Strand Reverse strand
Band p13.3
Transcripts
ENST00000315997 ENSP00000324672
ENST00000474471 ENSP00000417158
ENST00000472572 ENSP00000420566
ENST00000591875
ENST00000586629
ENST00000592343
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0042803 protein homodimerization activity
Biological Process
Cellular Component
GO:0005829 cytosol
GO:0016020 membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.11782
RefSeq NM_001098514 NM_152459 XM_005255143
HUGO
OMIM
CCDS CCDS42116 CCDS45404
HPRD 11353
IMGT
EMBL
GenPept
RNA Seq Atlas