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Symbol
Name
ID
Chromosome
D17Leh66D
DNA segment, Chr 17, Lehrach 66D
MGI:90718
17
16 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
Mapping Panel: Kozak FvC58 + FvSpr
17 J:49567 Gao JL, et al., Differential expansion of the N-formylpeptide receptor gene cluster in human and mouse. Genomics. 1998 Jul 15;51(2):270-6
CROSS Cross Type: Backcross
Mapping Panel: Kozak Skive (C58/J or NFS/N)
17 J:49567 Gao JL, et al., Differential expansion of the N-formylpeptide receptor gene cluster in human and mouse. Genomics. 1998 Jul 15;51(2):270-6
CROSS Cross Type: Backcross
17 J:9778 Hammer MF, et al., Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. Proc Natl Acad Sci U S A. 1989 May;86(9):3261-5
CROSS Cross Type: Backcross
17 J:9778 Hammer MF, et al., Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. Proc Natl Acad Sci U S A. 1989 May;86(9):3261-5
CROSS Cross Type: Intercross
17 J:460 King TR, et al., Meiotic mapping of murine chromosome 17: the string of loci around l(17)-2Pas. Mamm Genome. 1991;1(1):37-46
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:8163 Herrmann B, et al., Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes. Cell. 1986 Feb 14;44(3):469-76
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:3821 Noce T, et al., A novel murine zinc finger gene mapped within the tw18 deletion region expresses in germ cells and embryonic nervous system. Dev Biol. 1993 Feb;155(2):409-22
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
RI RI/RC Set: BXD
17 J:10135 Vincek V, et al., Linkage map of mouse chromosome 17: localization of 27 new DNA markers. Genomics. 1989 Nov;5(4):773-86
TEXT 17 J:50247 Bergstrom RA, et al., Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths. Genetics. 1998 Oct;150(2):815-22
TEXT 17 J:8163 Herrmann B, et al., Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes. Cell. 1986 Feb 14;44(3):469-76
TEXT 17 J:11036 Howard CA, et al., Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes. Genetics. 1990 Dec;126(4):1103-14
TEXT-Genetic Cross 17 J:9778 Hammer MF, et al., Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. Proc Natl Acad Sci U S A. 1989 May;86(9):3261-5
TEXT-Physical Mapping 17 J:42498 Schweifer N, et al., Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene. Genomics. 1997 Aug 1;43(3):285-97

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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory