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Echinobase

ECB-GENEPAGE-23075660
???displayGene.symbol??? :
 msx1
Symbol Status : Partially Curated


???displayGene.name???
msh homeobox 1
Name Status : Partially Curated


???displayGene.synonyms???
LOC110983414 , msh-like homeobox , Msx , Sp-Msx , SpMsx , SPU_022049 [+] ( Nomenclature history )

AI Protein Function :
The msx1 gene in Strongylocentrotus purpuratus encodes a transcription factor involved in embryonic development, including roles in skeletogenesis and neural development.



???displayGene.geneInteractants???
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Diseases: 


Disease Ontology:
orofacial cleft [+]

MIM:
TOOTH AGENESIS, SELECTIVE, 1; STHAG1 [+]

External Links:
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