AP3B1 protein, human

Preferred Label : AP3B1 protein, human;

MeSH note : Defects in AP3B1 are the cause of Hermansky-Pudlak syndrome type 2 (HPS2); RefSeq NM_003664;

MeSH synonym : HPS2 protein, human; adaptor-related protein complex 3, beta 1 subunit protein, human; beta3A-adaptin protein, human; ADTB3A protein, human; HPS-2 protein, human;

Is substance : O;

Détails

Origin ID

C439973;

UMLS CUI

C1099266;

MeSH indexing information
- hermanski-pudlak syndrome [MeSH Descriptor]
MeSH term(s) associated for indexing
- adaptor protein complex 3 [MeSH Descriptor]
- adaptor protein complex beta subunits [MeSH Descriptor]
Record concept(s)
- AP3B1 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- AP-3 Complex Subunit Beta-1 [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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