paralemmin 2 - CISMeF

Preferred Label : paralemmin 2;

Approved symbol HGNC : PALM2;

Chromosome HGNC : 9q31.3;

Locus type HGNC : other;

Origin ID

HGNC:15845;

UMLS CUI

C1423768;

Automatic exact mappings (from CISMeF team)
- Palm2 and akap2 fusion gene [OMIM gene]
- Paralemmin-2 [NCIt concept]
NCIt concept
- PALM2 Gene [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PALM2 Gene [NCIt concept]