- 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 |
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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