aptx protein, mouse

Preferred Label : aptx protein, mouse;

MeSH note : neurological disorders associated with APTX mutations may be caused by the gradual accumulation of unrepaired DNA strand breaks resulting from abortive DNA ligation events; RefSeq NM_025545.4, NP_079821.3 aprataxin isoform a; NM_001025444.2, NP_001020615.1 aprataxin isoform b;

CISMeF synonym : aprataxin protein isoform a, mouse; aprataxin protein isoform b, mouse;

MeSH synonym : aprataxin protein, mouse;

Is substance : O;

Details

Origin ID

C514665;

UMLS CUI

C1743807;

MeSH term(s) associated for indexing
- dna-binding proteins [MeSH Descriptor]
- nuclear proteins [MeSH Descriptor]
Record concept(s)
- aprataxin protein isoform a, mouse [MeSH concept]
- aprataxin protein isoform b, mouse [MeSH concept]
- aptx protein, mouse [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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