Tsc complex subunit 1

Preferred Label : Tsc complex subunit 1;

Symbol : TSC1;

CISMeF acronym : TSC1;

Type : Gene;

Alternative titles and symbols : HAMARTIN; Tsc1 gene;

Ensembl ID : ENSG00000165699;

Prefixed ID : *605284;

Details

Origin ID

605284;

UMLS CUI

C0694894;

Automatic exact mappings (from CISMeF team)
- C-C Motif Chemokine 26 [NCIt concept]
- CCL26 wt Allele [NCIt concept]
- Hamartin [NCIt concept]
- TSC complex subunit 1 [ORDO Gene]
- TSC complex subunit 1 [HGNC gene]
- TSC1 Gene [NCIt concept]
- TSC1 gene [LOINC component]
- TSC1 wt Allele [NCIt concept]
- Tuberous Sclerosis Complex 1 Protein [MeSH Descriptor]
HGNC gene
- TSC complex subunit 1 [HGNC gene]
NCIt concept(s)
- Hamartin [NCIt concept]
- TSC1 Gene [NCIt concept]
- TSC1 wt Allele [NCIt concept]
ORDO concept(s)
- TSC complex subunit 1 [ORDO Gene]
Phenotypes related
- Focal cortical dysplasia, type II [OMIM Phenotype]
- Lymphangioleiomyomatosis [OMIM Phenotype]
- Tuberous sclerosis 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TSC complex subunit 1 [HGNC gene]
- TSC1 Gene [NCIt concept]
- TSC1 gene [LOINC component]

Keyword's position in hierarchy(ies) :

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