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Resource:CASRDB- Calcium Sensing Receptor Database

Name: Resource:CASRDB- Calcium Sensing Receptor Database
Description:

CASRdb is a calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.

The information can be searched by mutation, genotype-phenotype, clinical data, in vitro analyses, and authors of publications describing the mutations. CASRdb is regularly updated for new mutations and it also provides a mutation submission form to ensure up-to-date information. The home page of this database provides links to different web pages that are relevant to the CASR, as well as disease clinical pages, sequence of the CASR gene exons, and position of mutations in the CASR. The CASRdb will help researchers to better understand and analyze the mutations, and aid in structure-function analyses.
Other Name(s): CASRDB
Parent Organization: McGill University; Montreal; Canada
Resource Type(s): Database
Resource: Resource
URL: http://www.casrdb.mcgill.ca/
*Id: nif-0000-02638
Keywords: familial hypocalciuric hypercalcemia, benign hypocalciuric hypercalcemia, calcium-sensing, hypocalciuric hypercalcemia, mutation causing hypocalciuric hypercalcemia
Link to OWL / RDF: Download this content as OWL/RDF

Curation status: Curated

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Contributors

Aarnaud, Ccdbuser, Eddy kim, Nifbot2



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Facts about Resource:CASRDB- Calcium Sensing Receptor DatabaseRDF feed
CurationStatusuncurated  +
DefiningCitationhttp://www.casrdb.mcgill.ca/  +
Definition

CASRdb is a calcium-sensing recept
CASRdb is a calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.

The information can be searched by mutation, genotype-phenotype, clinical data, in vitro analyses, and authors of publications describing the mutations. CASRdb is regularly updated for new mutations and it also provides a mutation submission form to ensure up-to-date information. The home page of this database provides links to different web pages that are relevant to the CASR, as well as disease clinical pages, sequence of the CASR gene exons, and position of mutations in the CASR. The CASRdb will help researchers to better understand and analyze the mutations, and aid in structure-function analyses.
aid in structure-function analyses.
Has default formThis property is a special property in this wiki.Resource  +
Has roleDatabase  +
Idnif-0000-02638  +
Is part ofMcGill University; Montreal; Canada  +
KeywordsFamilial hypocalciuric hypercalcemia  +, Benign hypocalciuric hypercalcemia  +, Calcium-sensing  +, Hypocalciuric hypercalcemia  +, and Mutation causing hypocalciuric hypercalcemia  +
LabelResource:CASRDB- Calcium Sensing Receptor Database  +
ModifiedDate20 June 2013  +
Page has default formThis property is a special property in this wiki.Resource  +
SuperCategoryResource  +
SynonymCASRDB  +