Chloride channel 7

Preferred Label : Chloride channel 7;

Symbol : CLCN7;

CISMeF acronym : CLCN7;

Type : Gene;

Alternative titles and symbols : CLC7;

Ensembl ID : ENSG00000103249;

Prefixed ID : *602727;

Details

Origin ID

602727;

UMLS CUI

C1413456;

Automatic exact mappings (from CISMeF team)
- CLCN7 Gene [NCIt concept]
- CLCN7 wt Allele [NCIt concept]
- H(+)/Cl(-) Exchange Transporter 7 [NCIt concept]
- chloride voltage-gated channel 7 [ORDO Gene]
- chloride voltage-gated channel 7 [HGNC gene]
HGNC gene
- chloride voltage-gated channel 7 [HGNC gene]
NCIt concept(s)
- CLCN7 Gene [NCIt concept]
- CLCN7 wt Allele [NCIt concept]
- H(+)/Cl(-) Exchange Transporter 7 [NCIt concept]
ORDO concept(s)
- chloride voltage-gated channel 7 [ORDO Gene]
Phenotypes related
- Hypopigmentation, organomegaly, and delayed myelination and development [OMIM Phenotype]
- Osteopetrosis, autosomal dominant 2 [OMIM Phenotype]
- Osteopetrosis, autosomal recessive 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CLCN7 Gene [NCIt concept]
- CLCN7 gene [LOINC component]
- chloride voltage-gated channel 7 [HGNC gene]

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