Symbol Name ID Chromosome |
D18Mit64
DNA segment, Chr 18, Massachusetts Institute of Technology 64 MGI:91119 18 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Backcross |
18 | J:39614 Erickson RP, et al., High-resolution mapping of the spm (Niemann-Pick Type C) locus on mouse chromosome 18. Mamm Genome. 1997 May;8(5):355-6 |
CROSS |
Cross Type: Backcross |
18 | J:33557 Griffith AJ, et al., Location of the 9257 and ataxia mutations on mouse chromosome 18. Mamm Genome. 1996 Jun;7(6):417-9 |
CROSS |
Cross Type: Backcross |
18 | J:64316 Hsu SJ, et al., Fine linkage and physical mapping suggests cross-over suppression with a retroposon insertion at the npc1 mutation. Mamm Genome. 2000 Sep;11(9):774-8 |
TEXT | 18 | J:39174 Smits R, et al., Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesis. Carcinogenesis. 1997 Feb;18(2):321-7 | |
TEXT-Genetic Cross | 18 | J:39614 Erickson RP, et al., High-resolution mapping of the spm (Niemann-Pick Type C) locus on mouse chromosome 18. Mamm Genome. 1997 May;8(5):355-6 | |
TEXT-Genetic Cross | 18 | J:39614 Erickson RP, et al., High-resolution mapping of the spm (Niemann-Pick Type C) locus on mouse chromosome 18. Mamm Genome. 1997 May;8(5):355-6 | |
TEXT-Genetic Cross | 18 | J:41469 Loftus SK, et al., Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene [see comments]. Science. 1997 Jul 11;277(5323):232-5 | |
TEXT-Genetic Cross | 18 | J:79322 Wilson SM, et al., Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease. Nat Genet. 2002 Nov;32(3):420-5 | |
TEXT-Physical Mapping | 18 | J:62826 Hsu SJ, et al., Construction of a long-range YAC physical map spanning the 10-cM region between the markers D18Mit109 and D18Mit68 on mouse proximal chromosome 18. Genome. 2000 Jun;43(3):427-33 | |
TEXT-Physical Mapping | 18 | J:64316 Hsu SJ, et al., Fine linkage and physical mapping suggests cross-over suppression with a retroposon insertion at the npc1 mutation. Mamm Genome. 2000 Sep;11(9):774-8 | |
TEXT-Physical Mapping | 18 | J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006; | |
TEXT-QTL | 18 | J:101740 Hollis-Moffatt JE, et al., Colocalization of mouse autoimmune diabetes loci Idd21.1 and Idd21.2 with IDDM6 (human) and Iddm3 (rat). Diabetes. 2005 Sep;54(9):2820-5 | |
TEXT-QTL | 18 | J:116664 Kesavan C, et al., Identification of genetic loci that regulate bone adaptive response to mechanical loading in C57BL/6J and C3H/HeJ mice intercross. Bone. 2006 Sep;39(3):634-43 | |
TEXT-QTL | 18 | J:98848 Lee GS, et al., A Gene(s) for All-trans-Retinoic Acid-Induced Forelimb Defects Mapped and Confirmed to Murine Chromosome 11. Genetics. 2005 May;170(1):345-53 | |
TEXT-Radiation Hybrid | 18 | J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004; |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/17/2024 MGI 6.24 |
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