Symbol Name ID Chromosome |
DXMit98
DNA segment, Chr X, Massachusetts Institute of Technology 98 MGI:95175 X |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Backcross |
X | J:63696 Blair HJ, et al., Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome. Mamm Genome. 2000 Aug;11(8):710-2 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83 |
CROSS |
Cross Type: Backcross |
X | J:33865 Sonin NV, et al., Molecular mapping of the mouse Gy mutation on Chromosome X. Mouse Genome. 1996;94(2):491-3 |
TEXT | X | J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55 | |
TEXT | X | J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55 | |
TEXT | X | J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55 | |
TEXT | X | J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31 | |
TEXT | X | J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31 | |
TEXT-Genetic Cross | X | J:79953 Carpinelli MR, et al., An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets. Am J Pathol. 2002 Nov;161(5):1925-33 | |
TEXT-Physical Mapping | X | J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006; | |
TEXT-Radiation Hybrid | X | 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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 12/10/2024 MGI 6.24 |
|
|