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.
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Diseases:
Disease Ontology:
orofacial cleft
MIM:
TOOTH AGENESIS, SELECTIVE, 1; STHAG1
External Links:
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Symbol legend: