Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1998-2-18
pubmed:abstractText
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 463 mutation entries from 406 unrelated families showing 303 unique molecular events. In addition to mutations, the database also lists variants or polymorphisms. Each patient is given a unique patient identity number (PIN). Information is included regarding the phenotype including symptoms. Mutations in all the five domains of BTK have been noticed to cause the disease, the most common event being missense mutations. The mutations appear almost uniformly throughout the molecule and frequently affect CpG sites that code for arginine residues. The putative structural implications of all the missense mutations are given in the database. The improved version of the registry having a number of new features is available at http://www. helsinki.fi/science/signal/btkbase.html
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-1280821, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-2307467, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-2877937, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-3003164, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7484460, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7519238, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7528500, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7576047, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7629518, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7633420, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7678927, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7711734, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7809124, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7849006, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7880320, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7927535, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7959728, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7970727, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-7989760, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8058772, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8070576, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8070814, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8090769, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8258324, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8283037, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8380905, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8421704, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8425221, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8435768, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8594569, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8885720, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8898377, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8914970, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8961623, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-8961625, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9016530, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9106525, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9110171, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9143921, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9192269, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9201297, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9218782, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9260159, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9280283, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9305846, http://linkedlifedata.com/resource/pubmed/commentcorrection/9399844-9399870
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0305-1048
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
242-7
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
pubmed:affiliation
Department of Biosciences, Division of Biochemistry, PO Box 56, FIN-00014 University of Helsinki, Finland. mauno.vihinen@helsinki.fi
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't