B6Brd;B6N-Tyrc-Brd Psat1tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12023 |
International strain name | B6Brd;B6N-Tyrc-Brd Psat1tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0151_3_G04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Psat1tm1a(KOMP)Wtsi, |
Gene/Transgene symbol | Psat1 |
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 EPD0151_3_G04. 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/6Dnk;C57BL/6Brd-Tyr |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Phosphoserine aminotransferase deficiency, infantile/juvenile form / Orphanet_284417
- Neu-Laxova syndrome / Orphanet_2671
- Neu-laxova syndrome due to phosphoserine aminotransferase deficiency / Orphanet_583602
IMPC phenotypes (allele matching)
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