IMPDH1, mouse - CISMeF

Preferred Label : IMPDH1, mouse;

MeSH note : mutant causes the RP10 form of autosomal dominant retinitis pigmentosa in mice;

MeSH synonym : inosine monophosphate dehydrogenase 1, mouse;

Registry Number MeSH : EC 1.1.1.205;

Is substance : O;

UNII : EC 1.1.1.205;

Details

Origin ID

C463299;

UMLS CUI

C1142734;

MeSH term(s) associated for indexing
- imp dehydrogenase [MeSH Descriptor]
Record concept(s)
- IMPDH1, mouse [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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