Piezo-type mechanosensitive ion channel component 1

Preferred Label : Piezo-type mechanosensitive ion channel component 1;

Symbol : PIEZO1;

CISMeF acronym : PIEZO1;

Type : Gene;

Alternative titles and symbols : Family with sequence similarity 38, member a; Membrane protein induced by beta-amyloid treatment; FAM38A; MIB;

Ensembl ID : ENSG00000103335;

Prefixed ID : *611184;

Details

Origin ID

611184;

UMLS CUI

C1539428;

Automatic exact mappings (from CISMeF team)
- MIB E3 ubiquitin protein ligase 1 [ORDO Gene]
- MIB1 wt Allele [NCIt concept]
- PIEZO1 Gene [NCIt concept]
- PIEZO1 wt Allele [NCIt concept]
- Piezo-Type Mechanosensitive Ion Channel Component 1 [NCIt concept]
- piezo type mechanosensitive ion channel component 1 [ORDO Gene]
- piezo type mechanosensitive ion channel component 1 (Er blood group) [HGNC gene]
HGNC gene
- piezo type mechanosensitive ion channel component 1 (Er blood group) [HGNC gene]
NCIt concept(s)
- PIEZO1 Gene [NCIt concept]
- PIEZO1 wt Allele [NCIt concept]
- Piezo-Type Mechanosensitive Ion Channel Component 1 [NCIt concept]
ORDO concept(s)
- piezo type mechanosensitive ion channel component 1 [ORDO Gene]
Phenotypes related
- Blood group, er [OMIM Phenotype]
- Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema [OMIM Phenotype]
- Lymphatic malformation 6 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PIEZO1 Gene [NCIt concept]
- piezo type mechanosensitive ion channel component 1 (Er blood group) [HGNC gene]

Keyword's position in hierarchy(ies) :

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