CLN3 protein, human

Preferred Label : CLN3 protein, human;

MeSH note : Defects in CLN3 are the cause of BATTEN DISEASE; also known as juvenile-onset ceroid lipofuscinosis neuronal type 3 (CLN3); RefSeq NM_000086;

MeSH synonym : ceroid-lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) protein, human; battenin protein, human; ceroid lipofuscinosis, neuronal 3 protein, human; Batten disease protein, human; Batten disease protein CLN3, human;

Is substance : O;

Details

Origin ID

C105199;

UMLS CUI

C0537445;

MeSH indexing information
- neuronal ceroid-lipofuscinoses [MeSH Descriptor]
MeSH term(s) associated for indexing
- membrane glycoproteins [MeSH Descriptor]
- molecular chaperones [MeSH Descriptor]
Record concept(s)
- CLN3 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)
- Battenin [NCIt concept]

Keyword's position in hierarchy(ies) :

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