- diluted coat color / MGI
- abnormal eye pigmentation / MGI
- abnormal blood coagulation / MGI
- no phenotypic analysis / MGI
- decreased platelet serotonin level / MGI
- abnormal melanosome morphology / MGI
- abnormal choroid pigmentation / MGI
- abnormal iris pigmentation / MGI
- abnormal retinal pigmentation / MGI
- immune system phenotype / MGI
- increased bleeding time / MGI
- absent eye pigmentation / MGI
- abnormal platelet dense granule physiology / MGI
- decreased platelet ATP level / MGI
- decreased platelet aggregation / MGI
- decreased platelet dense granule number / MGI
C57BL/6N-Atm1Brd Hps3tm2a(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:14381 |
Citation information | RRID:IMSR_EM:14381 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6N-Atm1Brd Hps3tm2a(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0907_2_H08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hps3tm2a(KOMP)Wtsi |
Gene/Transgene symbol | Hps3 |
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 EPD0907_2_H08. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hermansky-Pudlak syndrome without pulmonary fibrosis / Orphanet_231512
MGI phenotypes (gene matching)
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