NLM Logo

SOX9 Transcription Factor MeSH Descriptor Data 2022


MeSH Heading
SOX9 Transcription Factor
Tree Number(s)
D12.776.260.719.500.500
D12.776.660.235.400.750.500.500
D12.776.664.235.400.750.500.500
D12.776.930.823.500.500
Unique ID
D055758
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D055758
Scope Note
A SOXE transcription factor that plays a critical role in regulating CHONDROGENESIS; OSTEOGENESIS; and male sex determination. Loss of function of the SOX9 transcription factor due to genetic mutations is a cause of CAMPOMELIC DYSPLASIA.
Entry Term(s)
SOX-9 Transcription Factor
Registry Number
0
See Also
Pierre Robin Syndrome
Public MeSH Note
2009; SOX9 TRANSCRIPTION FACTOR was indexed under HIGH MOBILITY GROUP PROTEINS & TRANSCRIPTION FACTORS 1995-2008
History Note
2009(1995)
Entry Combination
deficiency:Campomelic Dysplasia
Date Established
2009/01/01
Date of Entry
2008/07/08
Revision Date
2014/06/13
SOX9 Transcription Factor Preferred
page delivered in 0.172s