T(7;18)50H
Cytogenetic Marker Detail

Symbol Name ID

T(7;18)50H reciprocal translocation, Chr 7 and 18, Harwell 50 MGI:103975

Synonyms

T50H

Feature Type

reciprocal chromosomal translocation

Genetic Map

Chromosome 7
cytoband E2

Alleles and phenotypes

All 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)   

Other database links

Entrez Gene

21266

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:23392 Beechey CV, List of Chromosome Anomalies. Mouse Genome. 1994;92:336-47
All references(12)

Other accession IDs

MGD-MRK-25297