SOX13

Source: Wikipedia, the free encyclopedia.
SOX13
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_005686

NM_011439

RefSeq (protein)

NP_005677

NP_035569

Location (UCSC)Chr 1: 204.07 – 204.13 MbChr 1: 133.31 – 133.35 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Transcription factor SOX-13 is a protein that in humans is encoded by the SOX13 gene.[5][6]

Function

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. It has also been determined to be a type-1 diabetes autoantigen, also known as islet cell antibody 12.[6]

In melanocytic cells SOX13 gene expression may be regulated by MITF.[7]

See also

  • SOX genes

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000143842Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070643Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. PMID 10198172
    .
  6. ^ a b "Entrez Gene: SOX13 SRY (sex determining region Y)-box 13".
  7. PMID 19067971
    .

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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