Mapping Data Summary

• Symbol: Ap3b1
• Name: adaptor-related protein complex 3, beta 1 subunit
• ID: MGI:1333879
• Chromosome: 13

35 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	13	J:7979 Elliott RW, et al., Linkage of loci affecting a murine liver protein and arylsulfatase B to chromosome 13. J Hered. 1985 Jul-Aug;76(4):243-6
CROSS	Cross Type: Backcross	13	J:7979 Elliott RW, et al., Linkage of loci affecting a murine liver protein and arylsulfatase B to chromosome 13. J Hered. 1985 Jul-Aug;76(4):243-6
CROSS	Cross Type: Backcross	13	J:747 Holcombe RF, et al., Linkage of loci associated with two pigment mutations on mouse chromosome 13. Genet Res. 1991 Aug;58(1):41-50
CROSS	Cross Type: Backcross	13	J:747 Holcombe RF, et al., Linkage of loci associated with two pigment mutations on mouse chromosome 13. Genet Res. 1991 Aug;58(1):41-50
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: 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: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: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: Backcross	13	J:32825 Poirier C, et al., The gene encoding the thrombin receptor (Cf2r) maps to mouse Chromosome 13. Mamm Genome. 1996 Apr;7(4):322
CROSS	Cross Type: Backcross	13	J:4110 Rikke BA, et al., Mus spretus-specific LINE-1 DNA probes applied to the cloning of the murine pearl locus. Genomics. 1993 Feb;15(2):291-6
CROSS	Cross Type: Backcross	13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
CROSS	Cross Type: Backcross	13	J:14314 Sweet HO, et al., Juvenile depilation (jd): a new hair loss mutation in the mouse. Mouse Genome. 1991;89:574-5
CROSS	Cross Type: Intercross	13	J:14314 Sweet HO, et al., Juvenile depilation (jd): a new hair loss mutation in the mouse. Mouse Genome. 1991;89:574-5
CROSS	Cross Type: Backcross	13	J:14314 Sweet HO, et al., Juvenile depilation (jd): a new hair loss mutation in the mouse. Mouse Genome. 1991;89:574-5
CROSS	Cross Type: Intercross	13	J:14314 Sweet HO, et al., Juvenile depilation (jd): a new hair loss mutation in the mouse. Mouse Genome. 1991;89:574-5
CROSS	Cross Type: Backcross	13	J:14314 Sweet HO, et al., Juvenile depilation (jd): a new hair loss mutation in the mouse. Mouse Genome. 1991;89:574-5
CROSS	Cross Type: Intercross	13	J:32739 Sweet HO, et al., Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. J Hered. 1996 Mar-Apr;87(2):87-95
CROSS	Cross Type: Intercross	13	J:32739 Sweet HO, et al., Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. J Hered. 1996 Mar-Apr;87(2):87-95
CROSS	Cross Type: Intercross	13	J:32739 Sweet HO, et al., Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. J Hered. 1996 Mar-Apr;87(2):87-95
CROSS	Cross Type: Intercross	13	J:32739 Sweet HO, et al., Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. J Hered. 1996 Mar-Apr;87(2):87-95
CROSS	Cross Type: Intercross	13	J:32739 Sweet HO, et al., Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. J Hered. 1996 Mar-Apr;87(2):87-95
TEXT		13	J:33579 Seymour AB, et al., An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Res. 1996 Jun;6(6):538-44
TEXT-Genetic Cross		13	J:52879 Feng L, et al., The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness. Hum Mol Genet. 1999 Feb;8(2):323-30
TEXT-Genetic Cross		13	J:747 Holcombe RF, et al., Linkage of loci associated with two pigment mutations on mouse chromosome 13. Genet Res. 1991 Aug;58(1):41-50
TEXT-Genetic Cross		13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
TEXT-Genetic Cross		13	J:33579 Seymour AB, et al., An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Res. 1996 Jun;6(6):538-44
TEXT-Genetic Cross		13	J:23861 Sweet HO, et al., Mesenchymal dysplasia (mes). Mouse News Lett. 1988;81:70
TEXT-Physical Mapping		13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;