Mapping Data Summary

• Symbol: Rara
• Name: retinoic acid receptor, alpha
• ID: MGI:97856
• Chromosome: 11

15 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	11	J:1082 Nadeau JH, et al., Close linkage of retinoic acid receptor genes with homeobox- and keratin-encoding genes on paralogous segments of mouse chromosomes 11 and 15. Mamm Genome. 1992;3(4):202-8
CROSS	Cross Type: Backcross	11	J:42692 Sato H, et al., A new mutation Rim3 resembling Re(den) is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11. Mamm Genome. 1998 Jan;9(1):20-25
CROSS	Cross Type: Backcross	11	J:42692 Sato H, et al., A new mutation Rim3 resembling Re(den) is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11. Mamm Genome. 1998 Jan;9(1):20-25
CROSS	Cross Type: Backcross Mapping Panel: Seldin	11	J:15814 Taketo M, et al., Mapping of the mouse Rar loci encoding retinoic acid receptors RAR alpha, RAR beta and RAR gamma. Jpn J Genet. 1993 Jun;68(3):175-84
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	11	J:63604 Wang W, et al., Identification of a novel chemokine (CCL28), which binds CCR10 (GPR2). J Biol Chem. 2000 Jul 21;275(29):22313-23
IN SITU	Band: D-E1	11	J:11474 Mattei MG, et al., Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomes. Genomics. 1991 Aug;10(4):1061-9
TEXT		11	J:54007 Sato H, et al., The genomic organization of type I keratin genes in mice. Genomics. 1999 Mar 15;56(3):303-9
TEXT		11	J:54007 Sato H, et al., The genomic organization of type I keratin genes in mice. Genomics. 1999 Mar 15;56(3):303-9
TEXT-Cytogenetic Localization		11	J:4100 Morris DJ, et al., Somatic cell hybrid mapping on mouse chromosome 11 (MMU11): assignment of markers relative to two breakpoints in band D. Genomics. 1993 Feb;15(2):323-31
TEXT-Cytogenetic Localization		11	J:39035 Squire JA, et al., Allelic fusion of DNA topoisomerase II alpha and retinoic acid receptor alpha genes in adriamycin-resistant p388 murine leukemia revealed by fluorescence in situ hybridization. Cytogenet Cell Genet. 1996;75(2-3):164-6
TEXT-Genetic Cross		11	J:79790 Kleiter N, et al., Mutagenic transgene insertion into a region of high gene density and multiple linkage disruptions on mouse chromosome 11. Cytogenet Genome Res. 2002;97(1-2):100-5
TEXT-QTL		11	J:36997 Fijneman RJ, et al., Complex interactions of new quantitative trait loci, Sluc1, Sluc2, Sluc3, and Sluc4, that influence the susceptibility to lung cancer in the mouse. Nat Genet. 1996 Dec;14(4):465-7
TEXT-QTL		11	J:98848 Lee GS, et al., A Gene(s) for All-trans-Retinoic Acid-Induced Forelimb Defects Mapped and Confirmed to Murine Chromosome 11. Genetics. 2005 May;170(1):345-53
TEXT-QTL		11	J:32079 Manenti G, et al., Genetic mapping of a pulmonary adenoma resistance (Par1) in mouse. Nat Genet. 1996 Apr;12(4):455-7
TEXT-QTL-Candidate Genes		11	J:91835 Kaput J, et al., Identification of genes contributing to the obese yellow Avy phenotype: caloric restriction, genotype, diet x genotype interactions. Physiol Genomics. 2004 Aug 11;18(3):316-24