B6Brd;B6N-Tyrc-Brd Pnpt1tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12137 |
International strain name | B6Brd;B6N-Tyrc-Brd Pnpt1tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0026_1_H08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Pnpt1tm1a(KOMP)Wtsi, |
Gene/Transgene symbol | Pnpt1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0026_1_H08. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Wellcome Trust Sanger Institute, Hinxton, United Kingdom |
Animals used for archiving | heterozygous C57BL/6J-Tyr |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
- Combined oxidative phosphorylation defect type 13 / Orphanet_319514
IMPC phenotypes (allele matching)
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