Source:http://linkedlifedata.com/resource/pubmed/id/10415331
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1-2
|
| pubmed:dateCreated |
1999-9-9
|
| pubmed:databankReference | |
| pubmed:abstractText |
The human Xq11-Xq21.3 region has been implicated in several inherited disorders including dystonia-parkinsonism (DYT3), sideroblastic anemia and several specific and non-specific forms of mental retardation (MR) syndromes. As part of a positional cloning effort to identify MR genes, we have generated a YAC-based transcript map. We first constructed a YAC/STS framework by extending previously published contigs. This framework map consists of a minimal set of 119 clones, covering approximately 20 Megabases (Mb) and allowing the precise ordering of 71 STSs between DXS136 and DXS472. This YAC contig was then used to define the positions of genes and expressed sequence tags (ESTs) assigned to the Xcen-Xq21.3 region. In addition to the genes previously localized to this part of the X chromosome, 18 transcription units corresponding to additional known genes or gene family members, one pseudogene and 15 novel transcripts were mapped. This transcriptional map incorporates 51 transcription units and provides a useful resource of candidate genes for some of the disorders assigned to this region of the X chromosome.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0378-1119
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
22
|
| pubmed:volume |
235
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
43-50
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| pubmed:dateRevised |
2011-11-17
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| pubmed:meshHeading |
pubmed-meshheading:10415331-Base Sequence,
pubmed-meshheading:10415331-Chromosomes, Artificial, Yeast,
pubmed-meshheading:10415331-Contig Mapping,
pubmed-meshheading:10415331-Databases, Factual,
pubmed-meshheading:10415331-Expressed Sequence Tags,
pubmed-meshheading:10415331-Genes,
pubmed-meshheading:10415331-Genetic Diseases, Inborn,
pubmed-meshheading:10415331-Genetic Linkage,
pubmed-meshheading:10415331-Humans,
pubmed-meshheading:10415331-Intellectual Disability,
pubmed-meshheading:10415331-Molecular Sequence Data,
pubmed-meshheading:10415331-Porins,
pubmed-meshheading:10415331-Pseudogenes,
pubmed-meshheading:10415331-RNA, Messenger,
pubmed-meshheading:10415331-Sequence Tagged Sites,
pubmed-meshheading:10415331-Transcription, Genetic,
pubmed-meshheading:10415331-Voltage-Dependent Anion Channels,
pubmed-meshheading:10415331-X Chromosome
|
| pubmed:year |
1999
|
| pubmed:articleTitle |
Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene.
|
| pubmed:affiliation |
INSERM U491, Génétique Médicale et Développement, Faculté de Médecine de la Timone, Université de la Méditerranée Marseille, 27 bd Jean Moulin, 13385, Marseille Cedex 5, France.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|