Mapping Data Summary

• Symbol: D13Mit9
• Name: DNA segment, Chr 13, Massachusetts Institute of Technology 9
• ID: MGI:89819
• Chromosome: 13

39 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:44483 Brady KP, et al., Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Res. 1997 Nov;7(11):1085-93
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:59118 Deak F, et al., Characterization and chromosome location of the mouse link protein gene (Crtl1). Cytogenet Cell Genet. 1999;87(1-2):75-9
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:4594 Eicher EM, et al., Molecular markers that define the distal ends of mouse autosomes 4, 13, and 19 and the sex chromosomes. Mamm Genome. 1993;4(4):226-9
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:47020 Greenberg RA, et al., Expression of mouse telomerase reverse transcriptase during development, differentiation and proliferation. Oncogene. 1998 Apr 2;16(13):1723-30
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:46071 Mjaatvedt CH, et al., Chondroitin sulfate proteoglycan 2 gene (Cspg2) is tightly linked to the heart defect (hdf) mouse locus on chromosome 13. MGI Direct Data Submission. 1998;
CROSS	Cross Type: Backcross	13	J:61322 Montgomery JC, et al., Chromosomal localization of the mouse G protein-coupled receptor kinase 5 and 6 genes. MGI Direct Data Submission. 2000;
CROSS	Cross Type: Backcross	13	J:29295 Naso MF, et al., Expression pattern and mapping of the murine versican gene (Cspg2) to chromosome 13. Genomics. 1995 Sep 1;29(1):297-300
CROSS	Cross Type: Backcross	13	J:22444 O'Brien EP, et al., Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD). Mamm Genome. 1995 Jan;6(1):19-24
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:60236 Pasteris NG, et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:60236 Pasteris NG, et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:24385 Roller ML, et al., Localization of sequences related to the human RAD6 DNA repair gene on mouse chromosomes 11 and 13. Mamm Genome. 1995 Apr;6(4):305-6
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:18140 Rowe LB, et al., Maps from two interspecific backcross DNA panels available as a community genetic mapping resource [published erratum appears in Mamm Genome 1994 Jul;5(7):463]. Mamm Genome. 1994 May;5(5):253-74
CROSS	Cross Type: Backcross	13	J:29377 Servadio A, et al., Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genes. Genomics. 1995 Oct 10;29(3):812-3
CROSS	Cross Type: Backcross	13	J:47657 Skradski SL, et al., Genetic mapping of a locus (mass1) causing audiogenic seizures in mice. Genomics. 1998 Apr 15;49(2):188-92
CROSS	Cross Type: Backcross	13	J:29850 Vinik BS, et al., Mapping of the MEK kinase gene (Mekk) to mouse chromosome 13 and human chromosome 5. Mamm Genome. 1995 Nov;6(11):782-3
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:41361 Wang W, et al., Otp maps to mouse chromosome 13. Mamm Genome. 1997 Jul;8(7):537-8
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:30838 Xu HP, et al., New polymorphic markers in the vicinity of the pearl locus on mouse chromosome 13. Mamm Genome. 1996 Jan;7(1):16-9
RI	RI/RC Set: BXD	13	J:1066 Dietrich W, et al., A genetic map of the mouse suitable for typing intraspecific crosses. Genetics. 1992 Jun;131(2):423-47
RI	RI/RC Set: BXH	13	J:138034 Misra V, et al., Mapping of MIT markers in the BXH RI panel. MGI Direct Data Submission. 2008;
RI	RI/RC Set: SMXA	13	J:30437 Nishimura M, et al., The SMXA: a new set of recombinant inbred strain of mice consisting of 26 substrains and their genetic profile. Mamm Genome. 1995 Dec;6(12):850-7
RI	RI/RC Set: HcB(N3)	13	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: HcB(N4)	13	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: CcS	13	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: AKXD	13	J:11923 Taylor BA, et al., Typing recombinant inbred mouse strains for microsatellite markers. Mamm Genome. 1993;4(5):239-42
TEXT-Genetic Cross		13	J:97534 Johnson KR, et al., The Mass1(frings) mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC. Genomics. 2005 May;85(5):582-90
TEXT-Genetic Cross		13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
TEXT-Genetic Cross		13	J:29377 Servadio A, et al., Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genes. Genomics. 1995 Oct 10;29(3):812-3
TEXT-Genetic Cross		13	J:33579 Seymour AB, et al., An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Res. 1996 Jun;6(6):538-44
TEXT-Genetic Cross		13	J:24193 Suda T, et al., Novel mouse microsatellites: primer sequences and chromosomal location. DNA Res. 1994;1(4):169-74
TEXT-Physical Mapping		13	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-QTL		13	J:93171 Cheverud JM, et al., Pleiotropic effects on mandibular morphology II: Differential epistasis and genetic variation in morphological integration. J Exp Zoolog Part A Comp Exp Biol. 2004 Sep 21;302B(5):424-35
TEXT-QTL		13	J:32208 Cheverud JM, et al., Quantitative trait loci for murine growth. Genetics. 1996 Apr;142(4):1305-19
TEXT-QTL		13	J:62610 Cheverud JM, et al., Genetic architecture of adiposity in the cross of LG/J and SM/J inbred mice. Mamm Genome. 2001 Jan;12(1):3-12
TEXT-QTL		13	J:70295 Ferraro TN, et al., Quantitative genetic study of maximal electroshock seizure threshold in mice: evidence for a major seizure susceptibility locus on distal chromosome 1. Genomics. 2001 Jul;75(1-3):35-42
TEXT-QTL		13	J:109795 Kenney-Hunt JP, et al., Quantitative trait loci for body size components in mice. Mamm Genome. 2006 Jun;17(6):526-37
TEXT-QTL		13	J:67526 Klingenberg C, et al., Genetic Architecture of Mandible Shape in Mice. Effects of quantitative trait loci analyzed by geometric morphometrics. Genetics. 2001 Feb;157(2):785-802
TEXT-QTL		13	J:42413 Leamy LJ, et al., A SEARCH FOR QUANTITATIVE TRAIT LOCI AFFECTING ASYMMETRY OF MANDIBULAR CHARACTERS IN MICE. Evolution. 1997 Jun;51(3):957-969
TEXT-QTL		13	J:53484 Leamy LJ, et al., Quantitative trait loci for early- and late-developing skull characters in mice: a test of the genetic independence model of morphological integration. Am Naturalist. 1999;153(2):201-214
TEXT-QTL		13	J:76126 Workman MS, et al., Analysis of quantitative trait locus effects on the size and shape of mandibular molars in mice. Genetics. 2002 Apr;160(4):1573-86