Piezo-type mechanosensitive ion channel component 2

Preferred Label : Piezo-type mechanosensitive ion channel component 2;

Symbol : PIEZO2;

CISMeF acronym : PIEZO2;

Type : Gene;

Alternative titles and symbols : Family with sequence similarity 38, member b; FAM38B;

Ensembl ID : ENSG00000154864;

Prefixed ID : *613629;

Details

Origin ID

613629;

UMLS CUI

C1539429;

Automatic exact mappings (from CISMeF team)
- PIEZO2 Gene [NCIt concept]
- PIEZO2 wt Allele [NCIt concept]
- Piezo-Type Mechanosensitive Ion Channel Component 2 [NCIt concept]
- piezo type mechanosensitive ion channel component 2 [ORDO Gene]
- piezo type mechanosensitive ion channel component 2 [HGNC gene]
HGNC gene
- piezo type mechanosensitive ion channel component 2 [HGNC gene]
NCIt concept(s)
- PIEZO2 Gene [NCIt concept]
- PIEZO2 wt Allele [NCIt concept]
- Piezo-Type Mechanosensitive Ion Channel Component 2 [NCIt concept]
ORDO concept(s)
- piezo type mechanosensitive ion channel component 2 [ORDO Gene]
Phenotypes related
- Arthrogryposis, distal, type 3 [OMIM Phenotype]
- Arthrogryposis, distal, type 5 [OMIM Phenotype]
- Arthrogryposis, distal, with impaired proprioception and touch [OMIM Phenotype]
- Marden-walker syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PIEZO2 Gene [NCIt concept]
- piezo type mechanosensitive ion channel component 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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