Mapping Data Summary

• Symbol: D17Leh94
• Name: DNA segment, Chr 17, Lehrach 94
• ID: MGI:90730
• Chromosome: 17

10 mapping experiments

Experiment Type	Details	Chromosome	Reference
RI	RI/RC Set: BXD	17	J:8922 Bucan M, et al., Deletion and duplication of DNA sequences is associated with the embryonic lethal phenotype of the t9 complementation group of the mouse t complex. Genes Dev. 1987 Jun;1(4):376-85
RI	RI/RC Set: BXD	17	J:14373 Crossley PH, et al., A cluster of related zinc finger protein genes is deleted in the mouse embryonic lethal mutation tw18. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7923-7
RI	RI/RC Set: BXD	17	J:11089 Friezner Degen SJ, et al., Characterization of the cDNA coding for mouse plasminogen and localization of the gene to mouse chromosome 17. Genomics. 1990 Sep;8(1):49-61
RI	RI/RC Set: BXD	17	J:11045 Nadeau JH, et al., Genetic maps of mouse chromosome 17 including 12 new anonymous DNA loci and 25 anchor loci. Genomics. 1991 Jan;9(1):78-89
RI	RI/RC Set: BXD	17	J:16826 Pauken CM, et al., Molecular cloning, expression analysis, and chromosomal localization of mouse Hmg1-containing sequences. Mamm Genome. 1994 Feb;5(2):91-9
RI	RI/RC Set: BXD	17	J:1578 Serikawa T, et al., Polymorphisms revealed by PCR with single, short-sized, arbitrary primers are reliable markers for mouse and rat gene mapping. Mamm Genome. 1992;3(2):65-72
TEXT		17	J:34878 Barclay J, et al., Physical analysis of the region deleted in the tw18 allele of the mouse tcl-4 complementation group. Genomics. 1996 Aug 15;36(1):39-46
TEXT		17	J:8922 Bucan M, et al., Deletion and duplication of DNA sequences is associated with the embryonic lethal phenotype of the t9 complementation group of the mouse t complex. Genes Dev. 1987 Jun;1(4):376-85
TEXT		17	J:36910 You Y, et al., Chromosomal deletion complexes in mice by radiation of embryonic stem cells. Nat Genet. 1997 Mar;15(3):285-8
TEXT-Physical Mapping		17	J:34878 Barclay J, et al., Physical analysis of the region deleted in the tw18 allele of the mouse tcl-4 complementation group. Genomics. 1996 Aug 15;36(1):39-46