Protein phosphatase 3, catalytic subunit, alpha isoform

Preferred Label : Protein phosphatase 3, catalytic subunit, alpha isoform;

Symbol : PPP3CA;

CISMeF acronym : PPP3CA;

Type : Gene;

Alternative titles and symbols : Calcineurin a; Calcineurin a1; Calcineurin a-alpha; Protein phosphatase 2b, catalytic subunit, alpha isoform; CALNA; CANA; CALNA1; CNA-ALPHA; PPP2B;

Ensembl ID : ENSG00000138814;

Prefixed ID : *114105;

Details

Origin ID

114105;

UMLS CUI

C1418845;

Automatic exact mappings (from CISMeF team)
- Calcineurin [NCIt concept]
- PPP3CA Gene [NCIt concept]
- PPP3CA wt Allele [NCIt concept]
- Protein phosphatase 3 [LOINC component]
- Protein phosphatase 3 (substance) [SNOMED CT concept]
- Serine/Threonine Protein Phosphatase 2B Catalytic Subunit Alpha Isoform [NCIt concept]
- calcineurin [MeSH concept]
- calcineurin [MeSH Descriptor]
- calcineurin A [MeSH concept]
- calcium-dependent protein serine/threonine phosphatase activity [GO term]
- protein phosphatase 3 catalytic subunit alpha [ORDO Gene]
- protein phosphatase 3 catalytic subunit alpha [HGNC gene]
- protein serine/threonine phosphatase activity [GO term]
HGNC gene
- protein phosphatase 3 catalytic subunit alpha [HGNC gene]
NCIt concept(s)
- PPP3CA Gene [NCIt concept]
- PPP3CA wt Allele [NCIt concept]
- Serine/Threonine Protein Phosphatase 2B Catalytic Subunit Alpha Isoform [NCIt concept]
ORDO concept(s)
- protein phosphatase 3 catalytic subunit alpha [ORDO Gene]
Phenotypes related
- Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development [OMIM Phenotype]
- Developmental and epileptic encephalopathy 91 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PPP3CA Gene [NCIt concept]
- protein phosphatase 3 catalytic subunit alpha [HGNC gene]

Keyword's position in hierarchy(ies) :

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