|  Help  |  About  |  Contact Us

Allele : Ptpn22<em1Shrm> protein tyrosine phosphatase, non-receptor type 22 (lymphoid); endonuclease-mediated mutation 1, Linda A Sherman
Primary Identifier  MGI:6149963 Allele Type  Endonuclease-mediated
Attribute String  Not Specified Gene  Ptpn22
Strain of Origin  NOD/ShiLtJ Is Recombinase  false
Is Wild Type  false
molecularNote  CRISPR-targeting generated a 4 nucleotide substitution in exon 14 that results in the amino acid substitution of tryptophan for arginine at position 619 (R619W). An additional silent mutation (CTC to CTT) was introduced at amino acid position 616.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Ptpn22<R619W>,
  • Ptpn22<R619W>
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

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

2 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