Spectrin, beta, nonerythrocytic, 1

Preferred Label : Spectrin, beta, nonerythrocytic, 1;

Symbol : SPTBN1;

CISMeF acronym : SPTBN1;

Type : Gene;

Alternative titles and symbols : Spectrin, nonerythroid, beta subunit; Beta-spectrin, general form; Beta-g spectrin; Fodrin, beta; Embryonic liver beta-fodrin; Spectrin, beta-II; SPTB2; ELF;

Ensembl ID : ENSG00000115306;

Prefixed ID : *182790;

Details

Origin ID

182790;

UMLS CUI

C1420388;

Automatic exact mappings (from CISMeF team)
- ELF Regimen [NCIt concept]
- Enhanced Liver Fibrosis Score [NCIt concept]
- SPTBN1 Gene [NCIt concept]
- SPTBN1 wt Allele [NCIt concept]
- Spectrin Beta Chain, Non-Erythrocytic 1 [NCIt concept]
- beta fodrin [MeSH concept]
- fodrin [MeSH Supplementary Concept]
- spectrin beta, non-erythrocytic 1 [HGNC gene]
HGNC gene
- spectrin beta, non-erythrocytic 1 [HGNC gene]
NCIt concept(s)
- SPTBN1 Gene [NCIt concept]
- SPTBN1 wt Allele [NCIt concept]
- Spectrin Beta Chain, Non-Erythrocytic 1 [NCIt concept]
ORDO concept(s)
- spectrin beta, non-erythrocytic 1 [ORDO Gene]
Phenotypes related
- Developmental delay, impaired speech, and behavioral abnormalities [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SPTBN1 Gene [NCIt concept]
- spectrin beta, non-erythrocytic 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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