- preweaning lethality, incomplete penetrance / IMPC
- abnormal vitreous body morphology / IMPC
- decreased locomotor activity / IMPC
- abnormal retina vasculature morphology / IMPC
- abnormal freezing behavior / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal retina blood vessel morphology / IMPC
STOCK Pcsk1tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:09998 |
Citation information | RRID:IMSR_EM:09998 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 | STOCK Pcsk1tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0508_1_C08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Pcsk1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Pcsk1 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0508_1_C08. For further details on the construction of this clone see the page at the IKMC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Obesity due to prohormone convertase I deficiency / Orphanet_71528
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- increased white adipose tissue amount / MGI
- hypoglycemia / MGI
- enlarged spleen / MGI
- increased body weight / MGI
- obese / MGI
- decreased body weight / MGI
- polyphagia / MGI
- chronic diarrhea / MGI
- reduced fertility / MGI
- abnormal spleen white pulp morphology / MGI
- abnormal spleen marginal zone morphology / MGI
- decreased circulating glucagon level / MGI
- decreased circulating insulin level / MGI
- abnormal hormone level / MGI
- transmission ratio distortion / MGI
- increased skeletal muscle mass / MGI
- decreased skeletal muscle mass / MGI
- decreased testis weight / MGI
- decreased mean systemic arterial blood pressure / MGI
- increased lymphocyte cell number / MGI
- decreased T cell number / MGI
- diarrhea / MGI
- decreased circulating growth hormone level / MGI
- decreased adrenocorticotropin level / MGI
- abnormal metabolism / MGI
- abnormal glucose tolerance / MGI
- impaired glucose tolerance / MGI
- insulin resistance / MGI
- abnormal inguinal fat pad morphology / MGI
- homeostasis/metabolism phenotype / MGI
- increased susceptibility to diet-induced obesity / MGI
- increased circulating leptin level / MGI
- decreased NK T cell number / MGI
- abnormal T-helper 1 cell differentiation / MGI
- decreased follicular dendritic cell number / MGI
- abnormal peritoneal macrophage morphology / MGI
- intermingled spleen red and white pulp / MGI
- slow postnatal weight gain / MGI
- increased circulating tumor necrosis factor level / MGI
- increased circulating interferon-gamma level / MGI
- increased circulating interleukin-10 level / MGI
- increased circulating interleukin-6 level / MGI
- increased circulating interleukin-12 level / MGI
- increased circulating interleukin-1 beta level / MGI
- increased interleukin-1 beta secretion / MGI
- increased susceptibility to endotoxin shock / MGI
- increased sensitivity to xenobiotic induced morbidity/mortality / MGI
- postnatal lethality, incomplete penetrance / MGI
- embryonic lethality before implantation, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
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