HLX (gene)

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

NM_021958

NM_008250

RefSeq (protein)

NP_068777

NP_032276

Location (UCSC)Chr 1: 220.88 – 220.89 MbChr 1: 184.46 – 184.46 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Homeobox Protein HB24 is a protein that in humans is encoded by the HLX gene.[5][6][7]

Role in development

Hlx belongs to the class of homeobox transcription factors, initially cloned from a B-lymphocyte cell line.

cardiogenic mesoderm. This is followed by signals from the septum transversum that induce epithelial-mesenchymal transition in the hepatic progenitors of the gut endoderm.[11][12] In a third stage, these signaling factors induce the liver endoderm to undergo proliferation and form liver cords. The same factor controls gut proliferation, and Hlx governs its expression. Although these mice develop anaemia, it is likely due to insufficient support from the liver in producing matrix component needed for hematopoiesis rather than an intrinsic defect in the hematopoietic cells.[9]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000136630Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000039377Ensembl, 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 1676597
    .
  6. .
  7. ^ "Entrez Gene: HLX1 H2.0-like homeobox 1 (Drosophila)".
  8. PMID 1672660
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  9. ^ .
  10. .
  11. .
  12. .

Further reading

External links

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