Sequestosome 1

Preferred Label : Sequestosome 1;

Symbol : SQSTM1;

CISMeF acronym : SQSTM1;

Type : Gene;

Alternative titles and symbols : Ubiquitin-binding protein p62; P62;

Ensembl ID : ENSG00000161011;

Prefixed ID : *601530;

Details

Origin ID

601530;

UMLS CUI

C1420393;

Automatic exact mappings (from CISMeF team)
- KHDRBS1 wt Allele [NCIt concept]
- SQSTM1 Gene [NCIt concept]
- SQSTM1 wt Allele [NCIt concept]
- Sequestosome-1 [NCIt concept]
- Sequestosome-1 Protein [MeSH Descriptor]
- nucleoporin 62 [ORDO Gene]
- sequestosome 1 [ORDO Gene]
- sequestosome 1 [HGNC gene]
HGNC gene
- sequestosome 1 [HGNC gene]
NCIt concept(s)
- SQSTM1 Gene [NCIt concept]
- SQSTM1 wt Allele [NCIt concept]
- Sequestosome-1 [NCIt concept]
ORDO concept(s)
- sequestosome 1 [ORDO Gene]
Phenotypes related
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 [OMIM Phenotype]
- Myopathy, distal, with rimmed vacuoles [OMIM Phenotype]
- Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset [OMIM Phenotype]
- Paget disease of bone 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SQSTM1 Gene [NCIt concept]
- sequestosome 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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