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T(7;18)50H
Cytogenetic Marker Detail
 Symbol
Name
ID
T(7;18)50H
reciprocal translocation, Chr 7 and 18, Harwell 50
MGI:103976
Synonyms T50H
Feature Type reciprocal chromosomal translocation
Genetic Map
Chromosome 18
cytoband B2

Mapping data(4)
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Radiation induced(1)
 
Mice heterozygous for this reciprocal translocation have reduced fertility. Unbalanced forms of this translocation comprising maternal or paternal duplication of Chr7 segments are used to study associated imprinted phenotypes.
 
Human Diseases Modeled Using Mouse T(7;18)50H (1)    Alleles Annotated to Human Diseases(1)    Phenotype Images(3)
Other database
links
Entrez Gene21267
References (Earliest) J:12947 Lyon MF, et al., The overall rates of dominant and recessive lethal and visible mutation induced by spermatogonial X-irradiation of mice. Genet Res. 1964;5:448-467
(Latest) J:198496 Resnick JL, et al., Recommendations for the investigation of animal models of Prader-Willi syndrome. Mamm Genome. 2013 Jun;24(5-6):165-78
All references(13)
Disease annotation references (2)
Other
accession IDs
MGD-MRK-25298

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
07/23/2014
MGI 5.19
The Jackson Laboratory