Mapping Data Summary

• Symbol: Foxq1
• Name: forkhead box Q1
• ID: MGI:1298228
• Chromosome: 13

20 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	13	J:23148 Avraham KB, et al., Murine chromosomal location of eight members of the hepatocyte nuclear factor 3/fork head winged helix family of transcription factors. Genomics. 1995 Jan 20;25(2):388-93
CROSS	Cross Type: Backcross	13	J:78730 Cheunsuk S, et al., Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility. J Autoimmun. 2002 Jun;18(4):311-6
CROSS	Cross Type: Backcross	13	J:10440 Dickinson ME, et al., Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci. Genomics. 1990 Mar;6(3):505-20
CROSS	Cross Type: Backcross	13	J:57749 Hansen GM, et al., Genetic profile of insertion mutations in mouse leukemias and lymphomas. Genome Res. 2000 Feb;10(2):237-43
CROSS	Cross Type: Backcross	13	J:4444 Hollander WF, Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse. J Hered. 1981 Sep-Oct;72(5):358-9
CROSS	Cross Type: Backcross	13	J:4444 Hollander WF, Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse. J Hered. 1981 Sep-Oct;72(5):358-9
CROSS	Cross Type: Backcross	13	J:4444 Hollander WF, Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse. J Hered. 1981 Sep-Oct;72(5):358-9
CROSS	Cross Type: Backcross	13	J:4444 Hollander WF, Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse. J Hered. 1981 Sep-Oct;72(5):358-9
CROSS	Cross Type: Backcross	13	J:10344 Justice MJ, et al., A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci. Genomics. 1990 Feb;6(2):341-51
CROSS	Cross Type: Backcross	13	J:5145 Lyon MF, et al., Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet Res. 1969 Oct;14(2):163-6
CROSS	Cross Type: Intercross	13	J:5145 Lyon MF, et al., Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet Res. 1969 Oct;14(2):163-6
CROSS	Cross Type: Backcross	13	J:5145 Lyon MF, et al., Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet Res. 1969 Oct;14(2):163-6
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: Unspecified	13	J:38300 Perou CM, et al., Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 1997 Jan 15;39(2):136-46
TEXT-Genetic Cross		13	J:78730 Cheunsuk S, et al., Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility. J Autoimmun. 2002 Jun;18(4):311-6
TEXT-Genetic Cross		13	J:49563 Frank S, et al., Mouse HNF-3/fork head homolog-1-like gene: structure, chromosomal location, and expression in adult and embryonic kidney. DNA Cell Biol. 1998 Aug;17(8):679-88
TEXT-Genetic Cross		13	J:5191 Green MC, The developmental effects of congenital hydrocephalus (ch) in the mouse. Dev Biol. 1970 Dec;23(4):585-608
TEXT-Physical Mapping		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Radiation Hybrid		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;