- increased exploration in new environment / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased hemoglobin content / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- decreased mean corpuscular volume / IMPC
- decreased circulating cholesterol level / IMPC
- abnormal skin condition / IMPC
- decreased circulating free fatty acids level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- decreased circulating HDL cholesterol level / IMPC
C57BL/6NTac-Rhdtm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:08733 |
International strain name | C57BL/6NTac-Rhdtm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0158_3_X01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Rhdtm1a(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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0158_3_X01. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Rh deficiency syndrome / Orphanet_71275
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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