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Strain Name:

STOCK gr +/+ Ap3d1mh/J

Stock Number:

000279

Availability:

Repository-Cryopreserved


Link to main datasheet for 000279

Additional References

 

Bloom JL; Falconer DS. 1966. "Grizzled", a mutant in linkage group X of the mouse. Genet Res 7:159-167.  [MGI Ref ID J:11987]

Bomar JM; Benke PJ; Slattery EL; Puttagunta R; Taylor LP; Seong E; Nystuen A; Chen W; Albin RL; Patel PD; Kittles RA; Sheffield VC; Burmeister M. 2003. Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse. (Erratum) Nat Genet 35(3):264-9. [PubMed: 14556008]  [MGI Ref ID J:85793]

Burwinkel B; Miglierini G; Jenne DE; Gilbert DJ; Copeland NG ; Jenkins NA ; Ring HZ ; Francke U ; Kilimann MW. 1998. Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice. Genomics 49(3):462-6. [PubMed: 9615234]  [MGI Ref ID J:47933]

Elewaut D; Lawton AP; Nagarajan NA; Maverakis E; Khurana A; Honing S; Benedict CA; Sercarz E; Bakke O; Kronenberg M; Prigozy TI. 2003. The adaptor protein AP-3 is required for CD1d-mediated antigen presentation of glycosphingolipids and development of Valpha14i NKT cells. J Exp Med 198(8):1133-46. [PubMed: 14557411]  [MGI Ref ID J:86243]

Falconer DS. 1950. Mutant stocks Mouse News Lett 2:3.  [MGI Ref ID J:24769]

Grabner CP; Price SD; Lysakowski A; Cahill AL; Fox AP. 2006. Regulation of large dense-core vesicle volume and neurotransmitter content mediated by adaptor protein 3. Proc Natl Acad Sci U S A 103(26):10035-40. [PubMed: 16788073]  [MGI Ref ID J:111070]

Jones SM; Erway LC; Johnson KR; Yu H; Jones TA. 2004. Gravity receptor function in mice with graded otoconial deficiencies. Hear Res 191(1-2):34-40. [PubMed: 15109702]  [MGI Ref ID J:89392]

Jones SM; Johnson KR; Yu H; Erway LC; Alagramam KN; Pollak N; Jones TA. 2005. A quantitative survey of gravity receptor function in mutant mouse strains. J Assoc Res Otolaryngol 6(4):297-310. [PubMed: 16235133]  [MGI Ref ID J:116914]

Kantheti P; Qiao X; Diaz ME; Peden AA; Meyer GE; Carskadon SL; Kapfhamer D; Sufalko D; Robinson MS; Noebels JL; Burmeister M. 1998. Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles. Neuron 21(1):111-22. [PubMed: 9697856]  [MGI Ref ID J:50662]

Lane PW; Deol MS. 1974. Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse. J Hered 65(6):362-4. [PubMed: 4448900]  [MGI Ref ID J:5511]

Miller CL; Burmeister M; Stevens KE. 1999. Hippocampal auditory gating in the hyperactive mocha mouse. Neurosci Lett 276(1):57-60. [PubMed: 10586974]  [MGI Ref ID J:59842]

Misawa H; Fujigaya H; Nishimura T; Moriwaki Y; Okuda T; Kawashima K; Nakata K; Ruggiero AM; Blakely RD; Nakatsu F; Ohno H. 2008. Aberrant trafficking of the high-affinity choline transporter in AP-3-deficient mice. Eur J Neurosci 27(12):3109-17. [PubMed: 18554297]  [MGI Ref ID J:137410]

Noebels JL; Sidman RL. 1989. Persistent hypersynchronization of neocortical neurons in the mocha mutant of mouse. J Neurogenet 6(1):53-6. [PubMed: 2778559]  [MGI Ref ID J:96307]

Qiao X; Pennesi M; Seong E; Gao H; Burmeister M; Wu SM. 2003. Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain. Vision Res 43(8):859-65. [PubMed: 12668055]  [MGI Ref ID J:88031]

Rolfsen RM; Erway LC. 1984. Trace metals and otolith defects in mocha mice. J Hered 75(3):159-62. [PubMed: 6736600]  [MGI Ref ID J:7485]

Salazar G; Craige B; Styers ML; Newell-Litwa KA; Doucette MM; Wainer BH; Falcon-Perez JM; Dell'Angelica EC; Peden AA; Werner E; Faundez V. 2006. BLOC-1 complex deficiency alters the targeting of adaptor protein complex-3 cargoes. Mol Biol Cell 17(9):4014-26. [PubMed: 16760431]  [MGI Ref ID J:114481]

Scheuber A; Rudge R; Danglot L; Raposo G; Binz T; Poncer JC; Galli T. 2006. Loss of AP-3 function affects spontaneous and evoked release at hippocampal mossy fiber synapses. Proc Natl Acad Sci U S A 103(44):16562-7. [PubMed: 17056716]  [MGI Ref ID J:115638]

Seong E; Wainer BH; Hughes ED; Saunders TL; Burmeister M; Faundez V. 2005. Genetic analysis of the neuronal and ubiquitous AP-3 adaptor complexes reveals divergent functions in brain. Mol Biol Cell 16(1):128-40. [PubMed: 15537701]  [MGI Ref ID J:94942]

Sevilla LM; Richter SS; Miller J. 2001. Intracellular transport of MHC class II and associated invariant chain in antigen presenting cells from AP-3-deficient mocha mice. Cell Immunol 210(2):143-53. [PubMed: 11520080]  [MGI Ref ID J:71349]

Silvers WK. 1979. The Coat Colors of Mice; A Model for Mammalian Gene Action and Interaction. In: The Coat Colors of Mice. Springer-Verlag, New York.  [MGI Ref ID J:78801]

Simpson F; Peden AA; Christopoulou L; Robinson MS. 1997. Characterization of the adaptor-related protein complex, AP-3. J Cell Biol 137(4):835-45. [PubMed: 9151686]  [MGI Ref ID J:20036]

Southard JL. 1970. Jackson circler, jc. Mouse News Lett 42:30.  [MGI Ref ID J:13506]

Swank RT; Novak EK; McGarry MP; Rusiniak ME; Feng L. 1998. Mouse models of Hermansky Pudlak syndrome: a review. Pigment Cell Res 11(2):60-80. [PubMed: 9585243]  [MGI Ref ID J:88018]

Swank RT; Novak EK; McGarry MP; Zhang Y; Li W; Zhang Q; Feng L. 2000. Abnormal vesicular trafficking in mouse models of Hermansky-Pudlak syndrome. Pigment Cell Res 13 Suppl 8:59-67. [PubMed: 11041359]  [MGI Ref ID J:103794]

Swank RT; Reddington M; Howlett O; Novak EK. 1991. Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha. Blood 78(8):2036-44. [PubMed: 1912584]  [MGI Ref ID J:29151]

 

Link to main datasheet for 000279

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