- decreased body weight / IMPC
- decreased heart weight / IMPC
- thrombocytopenia / IMPC
- decreased lean body mass / IMPC
- decreased NK cell number / IMPC
- decreased bone mineral content / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- increased or absent threshold for auditory brainstem response / IMPC
B6Brd;B6N-Tyrc-Brd Acsl4tm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:05887 |
International strain name | B6Brd;B6N-Tyrc-Brd Acsl4tm1a(EUCOMM)Wtsi/WtsiIeg |
Alternative name | EPD0066_2_D10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Acsl4tm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Acsl4 |
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 EUCOMM ES clone EPD0066_2_D10. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- X-linked non-syndromic intellectual disability / Orphanet_777
IMPC phenotypes (allele matching)
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