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IMPDH1, mouse MeSH Supplementary Concept Data 2025


MeSH Supplementary
IMPDH1, mouse
Unique ID
C463299
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C463299
Entry Term(s)
inosine monophosphate dehydrogenase 1, mouse
Registry Numbers
EC 1.1.1.205
Heading Mapped to
*IMP Dehydrogenase
Frequency
18
Note
mutant causes the RP10 form of autosomal dominant retinitis pigmentosa in mice
Source
Hum Mol Genet 2002 Mar 1;11(5)
Date of Entry
2002/08/16
Revision Date
2002/08/16
IMPDH1, mouse Preferred
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