Mapping Data Summary

• Symbol: Bloc1s5
• Name: biogenesis of lysosomal organelles complex-1, subunit 5, muted
• ID: MGI:2178598
• Chromosome: 13

19 mapping experiments

Experiment Type	Details	Chromosome	Reference
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: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: 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: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-Genetic Cross		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-Genetic Cross		13	J:23861 Sweet HO, et al., Mesenchymal dysplasia (mes). Mouse News Lett. 1988;81:70
TEXT-Genetic Cross		13	J:75830 Zhang Q, et al., The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Hum Mol Genet. 2002 Mar 15;11(6):697-706
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-Physical Mapping		13	J:75830 Zhang Q, et al., The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Hum Mol Genet. 2002 Mar 15;11(6):697-706