PROX1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Prospero homeobox protein 1 is a protein that in humans is encoded by the PROX1 gene.[5][6] The Prox1 gene is critical for the development of multiple tissues. Prox1 activity is necessary and sufficient to specify a lymphatic endothelial cell fate in endothelial progenitors located in the embryonic veins.[7]

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PROX1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPROX1, prospero homeobox 1
External IDsOMIM: 601546; MGI: 97772; HomoloGene: 2069; GeneCards: PROX1; OMA:PROX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001270616
NM_002763

NM_008937
NM_001360827

RefSeq (protein)

NP_001257545
NP_002754

NP_032963
NP_001347756

Location (UCSC)Chr 1: 213.98 – 214.04 MbChr 1: 189.85 – 189.9 Mb
PubMed search[3][4]
Wikidata
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Interactions

PROX1 has been shown to interact with EP300.[8]

Production

PROX1 is produced primarily in the dentate gyrus in the mouse, and in the dentate gyrus and white matter in humans. Gene expression data for mouse, human and macaque from the Allen Brain Atlases can be found here.

Clinical significance

PROX1 is used as a marker for lymphatic endothelium in biopsy samples. It has also been identified as an inhibitor of Müller glia (MG)-mediated retinal regeneration in mice that, when blocked from accessing MG cells, allowed retinal regeneration to occur, suggesting a possible therapeutic research pathway for drugs to treat degenerative diseases (such as retinitis pigmentosa) that lead to vision loss.[9]

Homologous gene

References

Further reading

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