Mapping Data Summary

• Symbol: Pax2
• Name: paired box 2
• ID: MGI:97486
• Chromosome: 19

17 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Unspecified	19	J:37055 Favor J, et al., The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13870-5
CROSS	Cross Type: Backcross	19	J:51693 Grimm C, et al., Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern. Dev Genet. 1998;23(4):299-316
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	19	J:49133 Hallonet M, et al., Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrain. Development. 1998 Jul;125(14):2599-610
CROSS	Cross Type: Backcross	19	J:29220 Johnson KR, et al., Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. Genomics. 1995 Sep 20;29(2):457-64
CROSS	Cross Type: Backcross Mapping Panel: JAX Mouse Mutant Resource BCB	19	J:29220 Johnson KR, et al., Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. Genomics. 1995 Sep 20;29(2):457-64
CROSS	Cross Type: Backcross	19	J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
CROSS	Cross Type: Backcross	19	J:11577 Walther C, et al., Pax: a murine multigene family of paired box-containing genes. Genomics. 1991 Oct;11(2):424-34
CROSS	Cross Type: Backcross	19	J:11577 Walther C, et al., Pax: a murine multigene family of paired box-containing genes. Genomics. 1991 Oct;11(2):424-34
CROSS	Cross Type: Backcross	19	J:11411 Yachou AK, et al., Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19. Genomics. 1991 Jul;10(3):531-8
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	19	J:46276 Yamashita T, et al., Genomic structure and chromosomal localization of the mouse LIM domain-binding protein 1 gene, Ldb1. Genomics. 1998 Feb 15;48(1):87-92
RI	RI/RC Set: Not Specified	19	J:26193 Mock BA, et al., CHUK, a conserved helix-loop-helix ubiquitous kinase, maps to human chromosome 10 and mouse chromosome 19. Genomics. 1995 May 20;27(2):348-51
TEXT		7	J:12104 Dressler GR, et al., Murine genes with homology to Drosophila segmentation genes. Development. 1988;104 Suppl:181-6
TEXT-Genetic Cross		19	J:42484 Gardner JM, et al., The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9238-43
TEXT-Genetic Cross		19	J:66458 Graw J, Mouse models of congenital cataract. Eye (Lond). 1999 Jun;13(Pt 3b):438-44
TEXT-Genetic Cross		19	J:51115 Hansen GM, et al., A mouse chromosome 19 genetic map including the Lvis1 viral insertion site. Genomics. 1999 Mar 1;56(2):228-31
TEXT-Genetic Cross		19	J:29220 Johnson KR, et al., Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. Genomics. 1995 Sep 20;29(2):457-64
TEXT-Genetic Cross		19	J:75964 Thaung C, et al., Novel ENU-induced eye mutations in the mouse: models for human eye disease. Hum Mol Genet. 2002 Apr 1;11(7):755-67