Mapping Data Summary

• Symbol: Myod1
• Name: myogenic differentiation 1
• ID: MGI:97275
• Chromosome: 7

37 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	7	J:15617 Brown SD, et al., Mapping the Hrc gene to proximal mouse chromosome 7: delineation of a conserved linkage group with human 19q. Genomics. 1993 Nov;18(2):459-61
CROSS	Cross Type: Backcross Mapping Panel: Seldin	7	J:28057 Butler A, et al., The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7. Immunogenetics. 1995;42(2):153-5
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross	7	J:10469 Cavanna JS, et al., Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q. Genomics. 1990 May;7(1):12-8
CROSS	Cross Type: Backcross Mapping Panel: Seldin	7	J:2945 Colombo MP, et al., Localization of growth arrest-specific genes on mouse chromosomes 1, 7, 8, 11, 13, and 16. Mamm Genome. 1992;2(2):130-4
CROSS	Cross Type: Backcross	7	J:1367 Handel MA, et al., Genetic approaches to analysis of LDH-C expression during spermatogenesis in the mouse. Isozyme Bulletin. 1992;25:36 (Abstr.)
CROSS	Cross Type: Backcross Mapping Panel: Seldin	7	J:44003 Hinson TK, et al., Identification of putative transmembrane receptor sequences homologous to the calcium-sensing G-protein-coupled receptor. Genomics. 1997 Oct 15;45(2):279-89
CROSS	Cross Type: Backcross	7	J:29904 Johnson DK, et al., Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. Genetics. 1995 Dec;141(4):1563-71
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:46206 Kalman K, et al., Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7. J Biol Chem. 1998 Mar 6;273(10):5851-7
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:3623 Leff SE, et al., Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat Genet. 1992 Dec;2(4):259-64
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:17629 Lock LF, et al., Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome. Genomics. 1994 Apr;20(3):354-62
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:22411 Lyman SD, et al., Identification of soluble and membrane-bound isoforms of the murine flt3 ligand generated by alternative splicing of mRNAs. Oncogene. 1995 Jan 5;10(1):149-57
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:31450 Nagasawa M, et al., Gene structure and chromosomal localization of the mouse NMDA receptor channel subunits. Brain Res Mol Brain Res. 1996 Feb;36(1):1-11
CROSS	Cross Type: Backcross	7	J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4
CROSS	Cross Type: Backcross Mapping Panel: Seldin	7	J:24219 Orr-Urtreger A, et al., Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor. Genomics. 1995 Mar 20;26(2):399-402
CROSS	Cross Type: Backcross	7	J:3600 Rinchik EM, et al., A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism. Nature. 1993 Jan 7;361(6407):72-6
CROSS	Cross Type: Backcross Mapping Panel: Seldin	7	J:10993 Saunders AM, et al., A molecular genetic linkage map of mouse chromosome 7. Genomics. 1990 Nov;8(3):525-35
CROSS	Cross Type: Backcross	7	J:30844 Stubbs L, et al., Location of the DBP transcription factor gene in human and mouse. Mamm Genome. 1996 Jan;7(1):65-7
CROSS	Cross Type: Backcross	7	J:34617 Stubbs L, et al., Detailed comparative map of human chromosome 19q and related regions of the mouse genome. Genomics. 1996 Aug 1;35(3):499-508
CROSS	Cross Type: Backcross	7	J:12638 Wright MD, et al., Gene structure, chromosomal localization, and protein sequence of mouse CD53 (Cd53): evidence that the transmembrane 4 superfamily arose by gene duplication. Int Immunol. 1993 Feb;5(2):209-16
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	7	J:17403 Wymore RS, et al., Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p1. Genomics. 1994 Mar 15;20(2):191-202
HYBRID		7	J:9415 Tapscott SJ, et al., MyoD1: a nuclear phosphoprotein requiring a Myc homology region to convert fibroblasts to myoblasts. Science. 1988 Oct 21;242(4877):405-11
TEXT		7	J:76777 Colinayo VV, et al., Genetic characterization of the Dyscalc locus. Mamm Genome. 2002 Jun;13(6):283-8
TEXT		7	J:38906 Dhar MS, et al., A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7. Mamm Genome. 1997 Feb;8(2):143-5
TEXT		7	J:29904 Johnson DK, et al., Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. Genetics. 1995 Dec;141(4):1563-71
TEXT		7	J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4
TEXT		7	J:29903 Russell LB, et al., Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. Genetics. 1995 Dec;141(4):1547-62
TEXT-Congenic		7	J:109580 Korff S, et al., Fine mapping of Dyscalc1, the major genetic determinant of dystrophic cardiac calcification in mice. Physiol Genomics. 2006 May 16;25(3):387-92
TEXT-Physical Mapping		7	J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-QTL		7	J:85812 Varga L, et al., Mapping modifiers affecting muscularity of the myostatin mutant (Mstn(Cmpt-dl1Abc)) compact mouse. Genetics. 2003 Sep;165(1):257-67
TEXT-Radiation Hybrid		7	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;