C57BL/6NTac-Aldh18a1tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12025 |
International strain name | C57BL/6NTac-Aldh18a1tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0071_1_D03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Aldh18a1tm1a(KOMP)Wtsi, |
Gene/Transgene symbol | Aldh18a1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0071_1_D03. 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/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant spastic paraplegia type 9B / Orphanet_447757
- Autosomal recessive spastic paraplegia type 9B / Orphanet_447760
- Autosomal dominant spastic paraplegia type 9A / Orphanet_447753
- ALDH18A1-related De Barsy syndrome / Orphanet_35664
- Autosomal dominant cutis laxa / Orphanet_90348
IMPC phenotypes (allele matching)
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).