- decreased circulating HDL cholesterol level / IMPC
- abnormal skin condition / IMPC
- decreased mean corpuscular volume / IMPC
- decreased circulating iron level / IMPC
- decreased circulating cholesterol level / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
B6Brd;B6N-Tyrc-Brd Rhdtm1e(EUCOMM)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:05430 |
International strain name | B6Brd;B6N-Tyrc-Brd Rhdtm1e(EUCOMM)Wtsi/WtsiOulu |
Alternative name | EPD0158_3_A08 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Rhdtm1e(EUCOMM)Wtsi, |
Gene/Transgene symbol | Rhd |
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 EPD0158_3_A08. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. Click here for more information on EUCOMM final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Rh deficiency syndrome / Orphanet_71275
IMPC phenotypes (allele matching)
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