Lamin b receptor

Preferred Label : Lamin b receptor;

Symbol : LBR;

CISMeF acronym : LBR;

Type : Gene;

Alternative titles and symbols : LMN2R;

Ensembl ID : ENSG00000143815;

Prefixed ID : *600024;

Details

Origin ID

600024;

UMLS CUI

C1416802;

Automatic exact mappings (from CISMeF team)
- Leidos Biomedical Research [NCIt concept]
- lamin B receptor [ORDO Gene]
- lamin B receptor [HGNC gene]
- lamin B receptor [MeSH concept]
False automatic mappings
- Liberia [NCIt concept]
HGNC gene
- lamin B receptor [HGNC gene]
NCIt concept(s)
- Delta(14)-Sterol Reductase LBR [NCIt concept]
- LBR Gene [NCIt concept]
- LBR wt Allele [NCIt concept]
ORDO concept(s)
- lamin B receptor [ORDO Gene]
Phenotypes related
- Greenberg dysplasia [OMIM Phenotype]
- Pelger-huet anomaly [OMIM Phenotype]
- Reynolds syndrome [OMIM Phenotype]
- Rhizomelic skeletal dysplasia with or without pelger-huet anomaly [OMIM Phenotype]
See also inter- (CISMeF)
- Lamin B Receptor [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LBR Gene [NCIt concept]
- lamin B receptor [HGNC gene]

Keyword's position in hierarchy(ies) :

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