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Symbol
Name
ID
Chromosome
D10Mit7
DNA segment, Chr 10, Massachusetts Institute of Technology 7
MGI:88854
10
21 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
10 J:37420 De Gregorio L, et al., Genetic mapping of thymine DNA glycosylase (Tdg) gene and of one pseudogene in the mouse. Mamm Genome. 1996 Dec;7(12):909-10
CROSS Cross Type: Backcross
Mapping Panel: EUCIB
10 J:17854 European Backcross Collaborative Group, Towards high resolution maps of the mouse and human genomes--a facility for ordering markers to 0.1 cM resolution. Hum Mol Genet. 1994 Apr;3(4):621-7
CROSS Cross Type: Backcross
10 J:18305 Irving NG, et al., Gene order is conserved within the human chromosome 21 linkage group on mouse chromosome 10. Genomics. 1994 May 1;21(1):144-9
CROSS Cross Type: Backcross
10 J:18305 Irving NG, et al., Gene order is conserved within the human chromosome 21 linkage group on mouse chromosome 10. Genomics. 1994 May 1;21(1):144-9
CROSS Cross Type: Backcross
10 J:21103 Kapfhamer D, et al., Genetic map of the region around grizzled (gr) and mocha (mh) on mouse chromosome 10, homologous to human 19p13.3. Genomics. 1994 Oct;23(3):635-42
CROSS Cross Type: Backcross
10 J:34619 Kapfhamer D, et al., The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3. Genomics. 1996 Aug 1;35(3):533-8
CROSS Cross Type: Other
10 J:34619 Kapfhamer D, et al., The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3. Genomics. 1996 Aug 1;35(3):533-8
CROSS Cross Type: Backcross
Mapping Panel: EUCIB (BSB)
10 J:26822 Kipling D, et al., YAC cloning Mus musculus telomeric DNA: physical, genetic, in situ and STS markers for the distal telomere of chromosome 10. Hum Mol Genet. 1995 Jun;4(6):1007-14
CROSS Cross Type: Backcross
10 J:45156 Kuroiwa A, et al., Association of tyrosine phosphatases SHP-1 and SHP-2, inositol 5-phosphatase SHIP with gp49B1, and chromosomal assignment of the gene. J Biol Chem. 1998 Jan 9;273(2):1070-4
CROSS Cross Type: Intercross
10 J:38429 Noben-Trauth K, et al., mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997 Sep 15;44(3):266-72
CROSS Cross Type: Backcross
Mapping Panel: EUCIB (BSS)
10 J:31574 Shiels A, et al., Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat Genet. 1996 Feb;12(2):212-5
CROSS Cross Type: Backcross
Mapping Panel: EUCIB (BSB)
10 J:31574 Shiels A, et al., Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat Genet. 1996 Feb;12(2):212-5
CROSS Cross Type: Backcross
Mapping Panel: EUCIB (both)
10 J:56632 Smith DP, et al., The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase. Hum Mol Genet. 1999 Aug;8(8):1479-85
CROSS Cross Type: Backcross
10 J:35469 Suzuki T, et al., Localization of mouse homolog of the bovine leukemia virus receptor gene on mouse chromosome 10. Mamm Genome. 1996 Sep;7(9):708-9
CROSS Cross Type: Backcross
Mapping Panel: UCLA (BSB)
10 J:34178 Welch CL, et al., Genetic regulation of cholesterol homeostasis: chromosomal organization of candidate genes. J Lipid Res. 1996 Jul;37(7):1406-21
RI RI/RC Set: OcB
10 J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
TEXT 10 J:85793 Bomar JM, et al., Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse. (Erratum). Nat Genet. 2003 Nov;35(3):264-9
TEXT-Genetic Cross 10 J:43160 Koike R, et al., Analysis of expression of lymphocyte homing-related adhesion molecules in ALY mice deficient in lymph nodes and Peyer's patches. Cell Immunol. 1997 Aug 25;180(1):62-9
TEXT-Genetic Cross 10 J:38429 Noben-Trauth K, et al., mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997 Sep 15;44(3):266-72
TEXT-Genetic Cross 10 J:103185 Samples R, et al., Tremor and reduced lifespan (trls): a new neurological mutation on Chromosome 10. MGI Direct Data Submission. 2005;
TEXT-Physical Mapping 10 J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;

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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory