Mapping Data Summary

• Symbol: Gli3
• Name: GLI-Kruppel family member GLI3
• ID: MGI:95729
• Chromosome: 13

37 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	13	J:28830 Brunialti AL, et al., The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13. Genomics. 1995 Sep 1;29(1):131-5
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:5123 Johnson DR, Brachyphalangy, an allele of extra-toes in the mouse. Genet Res. 1969 Jun;13(3):275-80
CROSS	Cross Type: Backcross	13	J:5123 Johnson DR, Brachyphalangy, an allele of extra-toes in the mouse. Genet Res. 1969 Jun;13(3):275-80
CROSS	Cross Type: Backcross	13	J:5123 Johnson DR, Brachyphalangy, an allele of extra-toes in the mouse. Genet Res. 1969 Jun;13(3):275-80
CROSS	Cross Type: Backcross	13	J:5123 Johnson DR, Brachyphalangy, an allele of extra-toes in the mouse. Genet Res. 1969 Jun;13(3):275-80
CROSS	Cross Type: Backcross	13	J:36920 Kingsmore SF, et al., Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13. J Investig Med. 1996 Oct;44(8):454-61
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: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: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: 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: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:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
CROSS	Cross Type: Backcross	13	J:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
CROSS	Cross Type: Backcross	13	J:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
CROSS	Cross Type: Backcross	13	J:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
CROSS	Cross Type: Backcross	13	J:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
CROSS	Cross Type: Backcross	13	J:5053 Lyon MF, et al., Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet Res. 1967 Jun;9(3):383-5
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
CROSS	Cross Type: Backcross	13	J:1958 Swank RT, et al., Sandy: a new mouse model for platelet storage pool deficiency. Genet Res. 1991 Aug;58(1):51-62
CROSS	Cross Type: Backcross	13	J:1958 Swank RT, et al., Sandy: a new mouse model for platelet storage pool deficiency. Genet Res. 1991 Aug;58(1):51-62
CROSS	Cross Type: Backcross	13	J:1958 Swank RT, et al., Sandy: a new mouse model for platelet storage pool deficiency. Genet Res. 1991 Aug;58(1):51-62
IN SITU	Band: A2	13	J:11318 Pohl TM, et al., Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt). Development. 1990 Dec;110(4):1153-7
TEXT		13	J:11318 Pohl TM, et al., Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt). Development. 1990 Dec;110(4):1153-7
TEXT		13	J:77245 Rachel RA, et al., A new allele of Gli3 and a new mutation, circletail (Crc), resulting from a single transgenic experiment. Genesis. 2002 Jun;33(2):55-61
TEXT-Genetic Cross		13	J:59913 Hudson JW, et al., Sak kinase gene structure and transcriptional regulation. Gene. 2000 Jan 4;241(1):65-73
TEXT-Genetic Cross		13	J:36920 Kingsmore SF, et al., Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13. J Investig Med. 1996 Oct;44(8):454-61
TEXT-Genetic Cross		13	J:70256 Martin N, et al., Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13. Genomics. 2001 Jul;75(1-3):9-16
TEXT-Genetic Cross		13	J:136642 Matera I, et al., A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Hum Mol Genet. 2008 Jul 15;17(14):2118-31
TEXT-Physical Mapping		13	J:75161 Kaiserman D, et al., Comparison of human chromosome 6p25 with mouse chromosome 13 reveals a greatly expanded ov-serpin gene repertoire in the mouse. Genomics. 2002 Mar;79(3):349-62
TEXT-Physical Mapping		13	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		13	J:28058 Martin B, et al., Mouse chromosomes 4 and 13 are involved in beta-carboline-induced seizures. J Hered. 1995 Jul-Aug;86(4):274-9
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;