Symbol Name ID Chromosome |
D10Mit138
DNA segment, Chr 10, Massachusetts Institute of Technology 138 MGI:88757 10 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Intercross |
10 | J:69655 Bryda EC, et al., High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (cdh23(v)). Genomics. 2001 May 1;73(3):338-42 |
TEXT | 10 | J:85407 Percec I, et al., An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse. Genetics. 2003 Aug;164(4):1481-94 | |
TEXT-Genetic Cross | 10 | J:38058 Bryda EC, et al., A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. Mamm Genome. 1997 Jan;8(1):1-4 | |
TEXT-Genetic Cross | 10 | J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003; | |
TEXT-Genetic Cross | 10 | J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003; | |
TEXT-Genetic Cross | 10 | J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7; | |
TEXT-Genetic Cross | 10 | J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7; | |
TEXT-Genetic Cross | 10 | J:97534 Johnson KR, et al., The Mass1(frings) mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC. Genomics. 2005 May;85(5):582-90 | |
TEXT-Genetic Cross | 10 | J:69985 Wilson SM, et al., Mutations in Cdh23 Cause Nonsyndromic Hearing Loss in waltzer Mice. Genomics. 2001 Jun 1;74(2):228-33 | |
TEXT-Physical Mapping | 10 | J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006; | |
TEXT-Physical Mapping | 10 | J:69985 Wilson SM, et al., Mutations in Cdh23 Cause Nonsyndromic Hearing Loss in waltzer Mice. Genomics. 2001 Jun 1;74(2):228-33 | |
TEXT-Radiation Hybrid | 10 | J:69655 Bryda EC, et al., High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (cdh23(v)). Genomics. 2001 May 1;73(3):338-42 |
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 |
|
|