RAB40AL protein, human

Preferred Label : RAB40AL protein, human;

MeSH note : mutations in this protein may be associated with mental retardation; may play a critical role in the development or function of the CNS, by transducing signals or transporting molecules across mitochondrial membranes; amino acid sequence in first source;

MeSH synonym : ras-like GTPase, human; RAB40A like protein, human; RLGP protein, human;

Registry Number MeSH : EC 3.6.1.-;

Is substance : O;

Details

Origin ID

C466300;

UMLS CUI

C1143954;

Automatic exact mappings (from CISMeF team)
- Fanconi Anemia Group J Protein [NCIt concept]
- Fanconi Anemia Group M Protein [NCIt concept]
- General Transcription and DNA Repair Factor IIH Helicase Subunit XPD [NCIt concept]
- RNA Helicase [NCIt concept]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
MeSH term(s) associated for indexing
- mitochondrial proteins [MeSH Descriptor]
- ras proteins [MeSH Descriptor]
Record concept(s)
- RAB40AL protein, human [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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