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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
Resource Type(s): database
Keywords: familial hypocalciuric hypercalcemia, benign hypocalciuric hypercalcemia, calcium-sensing, hypocalciuric hypercalcemia, mutation causing hypocalciuric hypercalcemia
Resource: Resource
URL: http://www.casrdb.mcgill.ca/
Id: nif-0000-02638
Link to OWL / RDF: Download this content as OWL/RDF

Curation status: Curated

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Retrieved from "http://neurolex.org/wiki/Category:Resource:CASRDB-_Calcium_Sensing_Receptor_Database"
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  +
KeywordsFamilial hypocalciuric hypercalcemia  +, Benign hypocalciuric hypercalcemia  +, Calcium-sensing  +, Hypocalciuric hypercalcemia  +, and Mutation causing hypocalciuric hypercalcemia  +
LabelResource:CASRDB- Calcium Sensing Receptor Database  +
ModifiedDate12 October 2010  +
SuperCategoryResource  +
SynonymCASRDB  +