heat shock protein family B (small) member 8

Preferred Label : heat shock protein family B (small) member 8;

Approved symbol HGNC : HSPB8;

Alias symbols HGNC : CMT2L; E2IG1; HSP22; H11;

Chromosome HGNC : 12q24.23;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000152137;

Details

Origin ID

HGNC:30171;

UMLS CUI

C1428937;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, axonal, type 2l [OMIM Phenotype]
- Heat-shock 22-kd protein 8 [OMIM gene]
- heat shock protein family B (small) member 8 [ORDO Gene]
NCIt concept
- HSPB8 Gene [NCIt concept]
OMIM gene
- Heat-shock 22-kd protein 8 [OMIM gene]
Orphanet gene
- heat shock protein family B (small) member 8 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HSPB8 Gene [NCIt concept]
- HSPB8 gene [LOINC component]
- Heat-shock 22-kd protein 8 [OMIM gene]

Keyword's position in hierarchy(ies) :

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