Symbol Name ID Chromosome |
D17Leh66D
DNA segment, Chr 17, Lehrach 66D MGI:90718 17 |
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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/05/2024 MGI 6.24 |
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