Chloride channel 5

Preferred Label : Chloride channel 5;

Symbol : CLCN5;

CISMeF acronym : CLCN5;

Type : Gene;

Alternative titles and symbols : Chloride channel, voltage-gated, k2; CLCK2; CLC5;

Ensembl ID : ENSG00000171365;

Prefixed ID : *300008;

Details

Origin ID

300008;

UMLS CUI

C1413454;

Automatic exact mappings (from CISMeF team)
- CLC-5 chloride channel [MeSH Supplementary Concept]
- CLCN5 gene [LOINC component]
- chloride voltage-gated channel 5 [ORDO Gene]
- chloride voltage-gated channel 5 [HGNC gene]
HGNC gene
- chloride voltage-gated channel 5 [HGNC gene]
NCIt concept(s)
- CLCN5 Gene [NCIt concept]
- CLCN5 wt Allele [NCIt concept]
- H(+)/Cl(-) Exchange Transporter 5 [NCIt concept]
ORDO concept(s)
- chloride voltage-gated channel 5 [ORDO Gene]
Phenotypes related
- Dent disease 1 [OMIM Phenotype]
- Hypophosphatemic rickets, X-linked recessive [OMIM Phenotype]
- Nephrolithiasis, X-linked recessive, with renal failure [OMIM Phenotype]
- Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CLCN5 Gene [NCIt concept]
- CLCN5 gene [LOINC component]
- chloride voltage-gated channel 5 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients