|  Help  |  About  |  Contact Us

Allele : Del(13)36H deletion, Chr 13, Harwell 36
Primary Identifier  MGI:3607783 Allele Type  Radiation induced
Gene  Del(13)36H Strain of Origin  (C3H/HeH x 101/H)F1
Is Recombinase  false Is Wild Type  false
molecularNote  This deletion, induced by X-irradiation of a (C3H/HeH x101/H)F1 female mouse, encompasses 12.66 Mb representing approximately 20% of mouse Chr 13 including bands A3.1 through A4. The deleted segment shares synteny with regions of human 6p25 and 6p22 associated with 6p deletion syndromes and 6p associated disorders.
  • mutations:
  • Intergenic deletion
  • synonyms:
  • Del(13)Svea36H,
  • Del36H,
  • Del36H,
  • Del(13)Svea36H
Paste the following link
Quick Links:
SummaryGenomePhenotypeOther
 
Quick Links:
SummaryGenomePhenotypeOther
 
Lists
This Allele isn't in any lists. Upload a list.

1 Feature

Trail: Allele

Genome

0 Expresses

467 Mutation Involves

Trail: Allele

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories

Trail: Allele




MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

© 2002 - 2017 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom