TLX1

Protein coding gene in Humans From Wikipedia, the free encyclopedia

T-cell leukemia homeobox protein 1 is a protein that in humans is encoded by the TLX1 gene, which was initially named HOX11.[5][6][7][8][9] As a transcription factor, TLX1 is involved in regulating which genes are transcribed, and therefore which proteins are produced by cells. In particular, it appears to be necessary for embryonic spleen development, since mice without a functional copy of the gene are born without a spleen. Chromosomal translocations of this gene can cause abnormal activation, and lead to T-cell leukemia, which is where the first part of the name comes from, while homeobox refers to the family of transcription factors it belongs to.[10]

AliasesTLX1, HOX11, TCL3, T-cell leukemia homeobox 1, T cell leukemia homeobox 1
End101,137,789 bp[1]
Quick facts Identifiers, Aliases ...
TLX1
Identifiers
AliasesTLX1, HOX11, TCL3, T-cell leukemia homeobox 1, T cell leukemia homeobox 1
External IDsOMIM: 186770; MGI: 98769; HomoloGene: 4031; GeneCards: TLX1; OMA:TLX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001195517
NM_005521

NM_021901

RefSeq (protein)

NP_001182446
NP_005512

n/a

Location (UCSC)Chr 10: 101.13 – 101.14 MbChr 19: 45.14 – 45.15 Mb
PubMed search[3][4]
Wikidata
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Interactions

TLX1 has been shown to interact with PPP1CC,[11] PPP2CB[11] and PPP2CA.[11]

References

Further reading

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