MEOX2

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

Mesenchyme homeobox 2 (MEOX2) is a protein that in humans is encoded by the MEOX2 gene.[5][6]

AliasesMEOX2, GAX, MOX2, mesenchyme homeobox 2
End15,686,683 bp[1]
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MEOX2
Identifiers
AliasesMEOX2, GAX, MOX2, mesenchyme homeobox 2
External IDsOMIM: 600535; MGI: 103219; HomoloGene: 4330; GeneCards: MEOX2; OMA:MEOX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005924

NM_008584

RefSeq (protein)

NP_005915

NP_032610

Location (UCSC)Chr 7: 15.61 – 15.69 MbChr 12: 37.16 – 37.23 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing transcription factor genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.[6] MEOX2 has been implicated in the initiation of tumors in glioma.[7] Additionally, MEOX2 influences several critical processes in lung cancer, including cellular proliferation, invasion, metastasis, angiogenesis, and the development of drug resistance.[8][9][10]

Interactions

MEOX2 has been shown to interact with PAX1[11] and PAX3.[11]

References

Further reading

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