ALS2 protein, human

Preferred Label : ALS2 protein, human;

MeSH note : mutated in a form of amyotrophic lateral sclerosis; Defects in ALS2 are the cause of AMYOTROPHIC LATERAL SCLEROSIS (ALS); RefSeq NM_020919;

MeSH synonym : amyotrophic lateral sclerosis 2 (juvenile) protein, human; alsin, human;

Is substance : O;

Details

Origin ID

C438187;

UMLS CUI

C1098466;

MeSH indexing information
- amyotrophic lateral sclerosis [MeSH Descriptor]
MeSH term(s) associated for indexing
- guanine nucleotide exchange factors [MeSH Descriptor]
Record concept(s)
- ALS2 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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