A 1.7-megabase sequence-ready cosmid contig covering the TSC1 candidate region in 9q34
- Univ. College London (United Kingdom); and others
The disease gene TSC1 has been genetically mapped to human chromosome region 9q34, in a 4-cM interval between the markers D9S149 and D9S114. Within this interval there is conflicting genetic evidence as to the finer localization of the gene. We have used finger-printing methods and hybridization to produce a 1.7-Mb overlapping clone map covering the TSC1. candidate region, with a single gap of 20 kb. We have localized 12 previously cloned genes and 17 genetic markers on this map and have confirmed the order of the genetic map. This deep set of overlapping clones is now ready to be used for candidate gene isolation, for transcription studies, or for sequencing. 27 refs., 3 figs.
- OSTI ID:
- 530734
- Journal Information:
- Genomics, Journal Name: Genomics Journal Issue: 3 Vol. 41; ISSN 0888-7543; ISSN GNMCEP
- Country of Publication:
- United States
- Language:
- English
Similar Records
A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig
Molecular analysis of tuberous sclerosis complex (TSC1) on chromosome 9q34
Mapping cosmid contigs to intervals on chromosome 9q34 by FISH
Journal Article
·
Sat Dec 31 23:00:00 EST 1994
· Genomics
·
OSTI ID:241066
Molecular analysis of tuberous sclerosis complex (TSC1) on chromosome 9q34
Journal Article
·
Thu Sep 01 00:00:00 EDT 1994
· American Journal of Human Genetics
·
OSTI ID:134428
Mapping cosmid contigs to intervals on chromosome 9q34 by FISH
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Thu Sep 01 00:00:00 EDT 1994
· American Journal of Human Genetics
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OSTI ID:134497
Related Subjects
55 BIOLOGY AND MEDICINE
BASIC STUDIES
BIOLOGICAL MARKERS
CONTIGS
COSMIDS
DESIGN
DNA SEQUENCING
DNA-CLONING
DOMINANT MUTATIONS
ELECTROPHORESIS
FLUORESCENCE
GENES
GENETIC MAPPING
HEREDITARY DISEASES
HUMAN CHROMOSOME 9
IN-SITU HYBRIDIZATION
MENTAL DISORDERS
PATIENTS
PHENOTYPE
RESOLUTION
SKIN DISEASES
TRANSCRIPTION
BASIC STUDIES
BIOLOGICAL MARKERS
CONTIGS
COSMIDS
DESIGN
DNA SEQUENCING
DNA-CLONING
DOMINANT MUTATIONS
ELECTROPHORESIS
FLUORESCENCE
GENES
GENETIC MAPPING
HEREDITARY DISEASES
HUMAN CHROMOSOME 9
IN-SITU HYBRIDIZATION
MENTAL DISORDERS
PATIENTS
PHENOTYPE
RESOLUTION
SKIN DISEASES
TRANSCRIPTION