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Symbol
Name
ID
Chromosome
D17Mit113
DNA segment, Chr 17, Massachusetts Institute of Technology 113
MGI:90753
17
23 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
17 J:31802 Gregorova S, et al., Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene. Mamm Genome. 1996 Feb;7(2):107-13
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
17 J:81452 Rantanen A, et al., Characterization of the mouse genes for mitochondrial transcription factors B1 and B2. Mamm Genome. 2003 Jan;14(1):1-6
RI RI/RC Set: EXCB
17 J:90435 Golas A, et al., Mapping of mouse Chromosome 4, 10, 12, 13, 15, 16, 17, 18, 19, X, STS markers in CBXE RI strains. MGI Direct Data Submission. 2004;
RI RI/RC Set: CBXE
17 J:90435 Golas A, et al., Mapping of mouse Chromosome 4, 10, 12, 13, 15, 16, 17, 18, 19, X, STS markers in CBXE RI strains. MGI Direct Data Submission. 2004;
RI RI/RC Set: CcS
17 J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
RI RI/RC Set: BXD
17 J:49829 Taylor BA, et al., Genotyping new BXD recombinant inbred mouse strains and comparison of BXD and consensus maps. Mamm Genome. 1999 Apr;10(4):335-48
TEXT 17 J:146599 Parvanov ED, et al., Trans-regulation of mouse meiotic recombination hotspots by Rcr1. PLoS Biol. 2009 Feb 17;7(2):e36
TEXT-Congenic 17 J:156885 Camateros P, et al., Identification of novel chromosomal regions associated with airway hyperresponsiveness in recombinant congenic strains of mice. Mamm Genome. 2010 Feb;21(1-2):28-38
TEXT-Congenic 17 J:237458 Street VA, et al., Resistance to noise-induced hearing loss in 129S6 and MOLF mice: identification of independent, overlapping, and interacting chromosomal regions. J Assoc Res Otolaryngol. 2014 Oct;15(5):721-38
TEXT-Genetic Cross 17 J:31802 Gregorova S, et al., Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene. Mamm Genome. 1996 Feb;7(2):107-13
TEXT-Genetic Cross 17 J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Genetic Cross 17 J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7;
TEXT-Genetic Cross 17 J:92463 JAX Reproductive Mutagenesis Program, Heritable mouse mutants from The Jackson Laboratory Reproductive Genomics Mutagenesis Program. MGI Direct Data Submission. 2004-7;
TEXT-Physical Mapping 17 J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-QTL 17 J:29366 Letts VA, et al., A curly-tail modifier locus, mct1, on mouse chromosome 17. Genomics. 1995 Oct 10;29(3):719-24
TEXT-QTL 17 J:111682 Mashimo T, et al., Two quantitative trait loci affecting progressive hearing loss in 101/H mice. Mamm Genome. 2006 Aug;17(8):841-50
TEXT-QTL 17 J:145148 Millward CA, et al., Genetic factors for resistance to diet-induced obesity and associated metabolic traits on mouse chromosome 17. Mamm Genome. 2009 Feb;20(2):71-82
TEXT-QTL 17 J:67838 Taylor BA, et al., Multiple obesity QTLs identified in an intercross between the NZO (New Zealand obese) and the SM (small) mouse strains. Mamm Genome. 2001 Feb;12(2):95-103
TEXT-QTL 17 J:71082 Williams RW, et al., Genetic dissection of the olfactory bulbs of mice: QTLs on four chromosomes modulate bulb size. Behav Genet. 2001 Jan;31(1):61-77
TEXT-QTL 17 J:80788 Yoshimura T, et al., Mapping quantitative trait loci affecting circadian photosensitivity in retinally degenerate mice. J Biol Rhythms. 2002 Dec;17(6):512-9
TEXT-Radiation Hybrid 17 J:71635 Li Q, et al., Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily. Gene. 2001 Aug 8;273(2):275-84
TEXT-Radiation Hybrid 17 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;
TEXT-Radiation Hybrid 17 J:76601 Tomac AC, et al., Assignment of the mouse Park2 (PARKIN), the homologue to a new human Parkinson candidate gene, to the telomeric region of mouse 17A3.2-3.3, by in situ hybridization. Cytogenet Cell Genet. 2001;95(1-2):120-1

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