C16orf89 (chromosome 16 open reading frame 89)

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Gene miRNA Gene ontology Other IDs Protein Related genes Diseases linked via similar genes

Gene

• Entrez ID: 146556
• Gene name: Chromosome 16 open reading frame 89
• Gene symbol: C16orf89
• Synonyms (NCBI Gene): -
• Chromosome: 16
• Chromosome location: 16p13.3
• 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

miRNA Show/Hide all (24)

miRTarBase ID	miRNA	Experiments	Reference
MIRT835579	hsa-miR-1293	CLIP-seq
MIRT835580	hsa-miR-31	CLIP-seq
MIRT835581	hsa-miR-3688-5p	CLIP-seq
MIRT835582	hsa-miR-4483	CLIP-seq
MIRT835583	hsa-miR-4731-5p	CLIP-seq
MIRT835584	hsa-miR-512-3p	CLIP-seq
MIRT1947606	hsa-miR-24	CLIP-seq
MIRT1947607	hsa-miR-3157-5p	CLIP-seq
MIRT1947608	hsa-miR-342-3p	CLIP-seq
MIRT1947609	hsa-miR-4284	CLIP-seq
MIRT1947610	hsa-miR-4691-3p	CLIP-seq
MIRT2185572	hsa-miR-1248	CLIP-seq
MIRT2185573	hsa-miR-1265	CLIP-seq
MIRT2185574	hsa-miR-1915	CLIP-seq
MIRT2185575	hsa-miR-4297	CLIP-seq
MIRT2185576	hsa-miR-4326	CLIP-seq
MIRT2185577	hsa-miR-4514	CLIP-seq
MIRT2185578	hsa-miR-4645-5p	CLIP-seq
MIRT2185579	hsa-miR-4673	CLIP-seq
MIRT2185580	hsa-miR-4691-5p	CLIP-seq
MIRT2185581	hsa-miR-4692	CLIP-seq
MIRT2185582	hsa-miR-4726-3p	CLIP-seq
MIRT2185583	hsa-miR-4764-5p	CLIP-seq
MIRT2185584	hsa-miR-4778-3p	CLIP-seq

Gene ontology (GO) Show/Hide all (7)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005576	Component	Extracellular region	IEA
GO:0005829	Component	Cytosol	IBA
GO:0005829	Component	Cytosol	IDA	20578903
GO:0016020	Component	Membrane	IBA
GO:0016020	Component	Membrane	IDA	20578903
GO:0042803	Function	Protein homodimerization activity	IPI	20578903
GO:0070062	Component	Extracellular exosome	HDA	19056867, 23533145

Other IDs

• MIM: 621148
• HGNC: 28687
• e!Ensembl: ENSG00000153446

Protein

• UniProt ID: Q6UX73
• Protein name: UPF0764 protein C16orf89
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF15882	DUF4735	60 → 334	Domain of unknown function (DUF4735)	Family

• Tissue specificity: TISSUE SPECIFICITY: Predominantly expressed in thyroid tissue. {ECO:0000269|PubMed:20578903}.
• Sequence:

  MASLGLLLLLLLTALPPLWSSSLPGLDTAESKATIADLILSALERATVFLEQRLPEINLD
  GMVGVRVLEEQLKSVREKWAQEPLLQPLSLRVGMLGEKLEAAIQRSLHYLKLSDPKYLRE
  FQLTLQPGFWKLPHAWIHTDASLVYPTFGPQDSFSEERSDVCLVQLLGTGTDSSEPCGLS
  DLCRSLMTKPGCSGYCLSHQLLFFLWARMRGCTQGPLQQSQDYINLFCANMMDLNRRAEA
  IGYAYPTRDIFMENIMFCGMGGFSDFYKLRWLEAILSWQKQQEGCFGEPDAEDEELSKAI
  QYQQHFSRRVKRREKQFPDSRSVAQAGVQWRNLGSLQPLPPGFKQFSCLILPSSWDYRSV
  PPYLANFYIFLVETGFHHVAHAGLELLISRDPPTSGSQSVGL

• Sequence length: 402

Related Genes

No strongly related genes found yet for C16orf89.

Diseases Linked via Similar Genes

No additional diseases found yet through genes similar to C16orf89.