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Msh homeobox 2

MSX2
Protein MSX2 PDB 1ig7.png
Identifiers
Aliases MSX2, CRS2, FPP, HOX8, MSH, PFM, PFM1, Msh homeobox 2
External IDs MGI: 97169 HomoloGene: 1837 GeneCards: MSX2
Gene location (Human)
Chromosome 5 (human)
Chr. Chromosome 5 (human)
Chromosome 5 (human)
Genomic location for MSX2
Genomic location for MSX2
Band 5q35.2 Start 174,724,533 bp
End 174,730,893 bp
RNA expression pattern
PBB GE MSX2 205555 s at fs.png

PBB GE MSX2 210319 x at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002449

NM_013601

RefSeq (protein)

NP_002440

NP_038629

Location (UCSC) Chr 5: 174.72 – 174.73 Mb Chr 5: 53.47 – 53.47 Mb
PubMed search

NM_002449

NM_013601

NP_002440

NP_038629

Homeobox protein MSX-2 is a protein that in humans is encoded by the MSX2 gene.

This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.

Msh homeobox 2 has been shown to interact with DLX5,DLX2 and MSX1.

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


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