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Symbol
Name
ID
Chromosome
Bloc1s6
biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
MGI:1927580
2
54 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
2 J:7208 Andrews SJ, et al., Linkage analyses and biochemical genetics of sorbitol dehydrogenase-1 (Sdh-1) in the mouse. Biochem Genet. 1983 Aug;21(7-8):809-17
CROSS Cross Type: Backcross
2 J:2 Bodmer WF, Viability effects and recombination differences in a linkage test with pallid and fidget in the house mouse. Heredity. 1961;16(4):485-95
CROSS Cross Type: Backcross
2 J:2 Bodmer WF, Viability effects and recombination differences in a linkage test with pallid and fidget in the house mouse. Heredity. 1961;16(4):485-95
CROSS Cross Type: Backcross
2 J:2 Bodmer WF, Viability effects and recombination differences in a linkage test with pallid and fidget in the house mouse. Heredity. 1961;16(4):485-95
CROSS Cross Type: Backcross
2 J:82 BORGER R, Order of genes in the 5th linkage group of the house mouse. Nature. 1950 Oct 21;166(4225):697
CROSS Cross Type: Backcross
2 J:86 Carter TC, et al., Ragged, a semidominant coat texture mutant. J Hered. 1954;45(4):151-154
CROSS Cross Type: Backcross
2 J:86 Carter TC, et al., Ragged, a semidominant coat texture mutant. J Hered. 1954;45(4):151-154
CROSS Cross Type: Backcross
2 J:3979 Davisson MT, et al., Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. Genetics. 1993 Mar;133(3):649-67
CROSS Cross Type: Backcross
2 J:3979 Davisson MT, et al., Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. Genetics. 1993 Mar;133(3):649-67
CROSS Cross Type: Backcross
2 J:3979 Davisson MT, et al., Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. Genetics. 1993 Mar;133(3):649-67
CROSS Cross Type: Backcross
2 J:3979 Davisson MT, et al., Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. Genetics. 1993 Mar;133(3):649-67
CROSS Cross Type: Backcross
2 J:3979 Davisson MT, et al., Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. Genetics. 1993 Mar;133(3):649-67
CROSS Cross Type: Backcross
2 J:10491 Davisson MT, et al., The mouse mutation ulnaless on chromosome 2. J Hered. 1990 Mar-Apr;81(2):151-3
CROSS Cross Type: Backcross
2 J:19416 Doute RC, et al., Tight-skin (Tsk) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15. Genomics. 1994 Jul 1;22(1):223-5
CROSS Cross Type: Backcross
2 J:247 FALCONER DS, Linkage in the mouse: the sex-linked genes and Rough. Z Indukt Abstamm Vererbungsl. 1954;86(2):263-8
CROSS Cross Type: Backcross
2 J:11021 Graff RJ, et al., Additional mapping of mouse chromosome 2 genes. Immunogenetics. 1991;33(2):96-100
CROSS Cross Type: Backcross
2 J:11021 Graff RJ, et al., Additional mapping of mouse chromosome 2 genes. Immunogenetics. 1991;33(2):96-100
CROSS Cross Type: Backcross
2 J:260 Green EL, et al., Opossum, a semi-dominant lethal mutation affecting hair and other characteristics of mice. J Hered. 1961;52(5):223-7
CROSS Cross Type: Backcross
2 J:5629 Green MC, et al., Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol. 1976 Mar;82(3):493-512
CROSS Cross Type: Backcross
2 J:5629 Green MC, et al., Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol. 1976 Mar;82(3):493-512
CROSS Cross Type: Backcross
2 J:5629 Green MC, et al., Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol. 1976 Mar;82(3):493-512
CROSS Cross Type: Backcross
2 J:5629 Green MC, et al., Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol. 1976 Mar;82(3):493-512
CROSS Cross Type: Intercross
2 J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
CROSS Cross Type: Backcross
2 J:8534 Hogan BL, et al., Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse. J Embryol Exp Morphol. 1986 Sep;97(1):95-110
CROSS Cross Type: Backcross
2 J:1621 Juriloff DM, et al., Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2. J Hered. 1991 Sep-Oct;82(5):402-5
CROSS Cross Type: Backcross
2 J:1621 Juriloff DM, et al., Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2. J Hered. 1991 Sep-Oct;82(5):402-5
CROSS Cross Type: Backcross
2 J:1621 Juriloff DM, et al., Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2. J Hered. 1991 Sep-Oct;82(5):402-5
CROSS Cross Type: Intercross
2 J:4455 Lilly F, The location of histocompatibility-6 in the mouse genome. Transplantation. 1967;5(1):83-85
CROSS Cross Type: Intercross
2 J:7689 Maltais LJ, et al., Anorexia, a recessive mutation causing starvation in preweanling mice. J Hered. 1984 Nov-Dec;75(6):468-72
CROSS Cross Type: Backcross
2 J:7471 Martin SA, et al., Histidine decarboxylase phenotypes of inbred mouse strains: a regulatory locus (Hdc) determines kidney enzyme concentration. Biochem Genet. 1984 Apr;22(3-4):305-22
CROSS Cross Type: Backcross
2 J:8676 Middleton RJ, et al., A new regulatory gene in the histidine decarboxylase gene complex determines the responsiveness of the mouse kidney enzyme to testosterone. Genet Res. 1987 Feb;49(1):61-7
CROSS Cross Type: Backcross
2 J:10040 Peters J, et al., Localization of Blvr, biliverdin reductase, on mouse chromosome 2. Genomics. 1989 Aug;5(2):270-4
CROSS Cross Type: Backcross
2 J:10040 Peters J, et al., Localization of Blvr, biliverdin reductase, on mouse chromosome 2. Genomics. 1989 Aug;5(2):270-4
CROSS Cross Type: Backcross
2 J:293 Roberts E, et al., Linkage of the genes for non-yellow (y) and pink-eye (p2) in the house mouse (Mus musculus). Am Naturalist. 1935;69:181-3
CROSS Cross Type: Backcross
2 J:293 Roberts E, et al., Linkage of the genes for non-yellow (y) and pink-eye (p2) in the house mouse (Mus musculus). Am Naturalist. 1935;69:181-3
CROSS Cross Type: Backcross
2 J:6707 Robinson PJ, et al., Location of the mouse beta 2-microglobulin gene B2m determined by linkage analysis. Immunogenetics. 1981;14(5):449-52
CROSS Cross Type: Backcross
2 J:115 Snell GD, An Analysis of Translocations in the Mouse. Genetics. 1946 Mar;31(2):157-80
CROSS Cross Type: Backcross
2 J:115 Snell GD, An Analysis of Translocations in the Mouse. Genetics. 1946 Mar;31(2):157-80
CROSS Cross Type: Backcross
2 J:8794 Taylor BA, et al., Localization of the inosine triphosphatase locus (Itp) on chromosome 2 of the mouse. Biochem Genet. 1987 Apr;25(3-4):267-74
CROSS Cross Type: Backcross
2 J:8242 West JD, et al., Further experience of the mouse dominant cataract mutation test from an experiment with ethylnitrosourea. Mutat Res. 1986 Apr;164(2):127-36
TEXT 2 J:252 Fisher RA, et al., Sex differences of crossing-over in close linkage. Am Naturalist. 1953;87:116
TEXT 2 J:18840 Graff RJ, et al., Continued mapping of chromosome 2 genes. Immunogenetics. 1994;40(1):21-6
TEXT 2 J:11021 Graff RJ, et al., Additional mapping of mouse chromosome 2 genes. Immunogenetics. 1991;33(2):96-100
TEXT 2 J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
TEXT 2 J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
TEXT-Genetic Cross 2 J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
TEXT-Genetic Cross 2 J:13936 Maltais L, et al., Anorexia (anx). Mouse News Lett. 1983;68:72
TEXT-Genetic Cross 2 J:6960 Meruelo D, et al., Evidence for a major cluster of lymphocyte differentiation antigens on murine chromosome 2. Proc Natl Acad Sci U S A. 1982 Dec;79(23):7460-4
TEXT-Genetic Cross 2 J:2185 White RA, et al., The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nat Genet. 1992 Sep;2(1):80-3
TEXT-Physical Mapping 2 J:43841 Huang L, et al., A novel gene involved in zinc transport is deficient in the lethal milk mouse. Nat Genet. 1997 Nov;17(3):292-7
TEXT-Physical Mapping 2 J:64907 Huang L, et al., The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency. Nat Genet. 1999 Nov;23(3):329-32
TEXT-Physical Mapping 2 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 2 J:116665 Yu X, et al., Fine mapping of collagen-induced arthritis quantitative trait loci in an advanced intercross line. J Immunol. 2006 Nov 15;177(10):7042-9
TEXT-Radiation Hybrid 2 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory