Mapping Data Summary

• Symbol: D19Mit32
• Name: DNA segment, Chr 19, Massachusetts Institute of Technology 32
• ID: MGI:91242
• Chromosome: 19

28 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:54028 Brady KP, et al., A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics. 1999 Mar 15;56(3):254-61
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	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: Intercross	19	J:84147 Dunnwald M, et al., The ichq mutant mouse, a model for the human skin disorder harlequin ichthyosis: mapping, keratinocyte culture, and consideration of candidate genes involved in epidermal growth regulation. Exp Dermatol. 2003 Jun;12(3):245-254
CROSS	Cross Type: Backcross	19	J:32962 Elliott RW, Errata for the Mouse Genetic Maps at Whitehead/MIT. MGI Direct Data Submission. 1996-04;
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:50321 Fowler KJ, et al., Genetic mapping of mouse centromere protein (Incenp and Cenpe) genes. Cytogenet Cell Genet. 1998;82(1-2):67-70
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:38984 Lopez-Nieto CE, et al., Molecular cloning and characterization of NKT, a gene product related to the organic cation transporter family that is almost exclusively expressed in the kidney. J Biol Chem. 1997 Mar 7;272(10):6471-8
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:38984 Lopez-Nieto CE, et al., Molecular cloning and characterization of NKT, a gene product related to the organic cation transporter family that is almost exclusively expressed in the kidney. J Biol Chem. 1997 Mar 7;272(10):6471-8
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:70373 Mills M, et al., Differential expression of the actin-binding proteins, alpha-actinin-2 and -3, in different species: implications for the evolution of functional redundancy. Hum Mol Genet. 2001 Jun 15;10(13):1335-46
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:56259 Mintz L, et al., EHD1--an EH-domain-containing protein with a specific expression pattern. Genomics. 1999 Jul 1;59(1):66-76
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:48183 Rahman A, et al., Two kinesin light chain genes in mice. Identification and characterization of the encoded proteins. (Erratum pg. 24280). J Biol Chem. 1998 Jun 19;273(25):15395-403
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:37421 Rowe LB, et al., Genetic mapping of 18S ribosomal RNA-related loci to mouse chromosomes 5, 6, 9, 12, 17, 18, 19, and X. Mamm Genome. 1996 Dec;7(12):886-9
CROSS	Cross Type: Backcross	19	J:22796 Sebastiani G, et al., Localization of the Catf1 transcription factor gene to mouse chromosome 19. Mamm Genome. 1995 Feb;6(2):147-8
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:42524 Stankewich MC, et al., A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles. Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14158-63
CROSS	Cross Type: Backcross	19	J:37823 Tchernev VT, et al., Genetic mapping of 20 novel expressed sequence tags from midgestation mouse embryos suggests chromosomal clustering. Genomics. 1997 Feb 15;40(1):170-4
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:39608 Wright A, et al., Mart1 is located on mouse chromosome 19 and is excluded as a candidate for ep and ru. Mamm Genome. 1997 May;8(5):377-8
RI	RI/RC Set: AXB	19	J:36911 Naggert JK, et al., An additional 136 SSLP markers typed for the AXB and BXA recombinant inbred mouse strains. Mamm Genome. 1997 Mar;8(3):209-11
RI	RI/RC Set: BXA	19	J:36911 Naggert JK, et al., An additional 136 SSLP markers typed for the AXB and BXA recombinant inbred mouse strains. Mamm Genome. 1997 Mar;8(3):209-11
RI	RI/RC Set: SWXJ	19	J:34480 Shultz KL, et al., Strain distribution pattern for SSLP markers in the SWXJ recombinant inbred strain set: chromosomes 7 to X. Mamm Genome. 1996 Jul;7(7):526-32
RI	RI/RC Set: OcB	19	J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
TEXT		19	J:51890 Cox GA, et al., Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron. 1998 Dec;21(6):1327-37
TEXT-Genetic Cross		19	J:22828 Casteels D, et al., The mouse Fau gene: genomic structure, chromosomal localization, and characterization of two retropseudogenes. Genomics. 1995 Jan 1;25(1):291-4
TEXT-Genetic Cross		19	J:32962 Elliott RW, Errata for the Mouse Genetic Maps at Whitehead/MIT. MGI Direct Data Submission. 1996-04;
TEXT-Genetic Cross		19	J:61295 Scimeca JC, et al., The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants. Bone. 2000 Mar;26(3):207-13
TEXT-Physical Mapping		19	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Physical Mapping		19	J:61295 Scimeca JC, et al., The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants. Bone. 2000 Mar;26(3):207-13
TEXT-QTL		19	J:68402 Suzuki T, et al., Quantitative trait locus analysis of abnormal circadian period in CS mice. Mamm Genome. 2001 Apr;12(4):272-7
TEXT-QTL		19	J:81573 Youngren KK, et al., Testicular cancer susceptibility in the 129.MOLF-Chr19 mouse strain: additive effects, gene interactions and epigenetic modifications. Hum Mol Genet. 2003 Feb 15;12(4):389-98
TEXT-Radiation Hybrid		19	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;