lamin B2 - CISMeF

Preferred Label : lamin B2;

Approved symbol HGNC : LMNB2;

Chromosome HGNC : 19p13.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000176619;

Details

Origin ID

HGNC:6638;

UMLS CUI

C1416878;

Automatic exact mappings (from CISMeF team)
- Lamin b2 [OMIM gene]
- lamin B2 [ORDO Gene]
- lamin B2 [MeSH Supplementary Concept]
- lamin B2 [MeSH concept]
OMIM gene
- Lamin b2 [OMIM gene]
Orphanet gene
- lamin B2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Lamin b2 [OMIM gene]

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