IMPC phenotypes (allele matching)
- preweaning lethality, complete penetrance / IMPC
C57BL/6NTac-Senp1em1(IMPC)H/H
| Status | Available to order |
| EMMA ID | EM:13354 |
| International strain name | C57BL/6NTac-Senp1em1(IMPC)H/H |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Senp1em1(IMPC)H |
| Gene/Transgene symbol | Senp1 |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
MGI phenotypes (gene matching)
- abnormal erythropoiesis / MGI
- abnormal vascular development / MGI
- abnormal cell death / MGI
- small liver / MGI
- pale liver / MGI
- abnormal liver physiology / MGI
- anemia / MGI
- prenatal lethality / MGI
- abnormal megakaryocyte progenitor cell morphology / MGI
- decreased erythrocyte cell number / MGI
- no phenotypic analysis / MGI
- abnormal vitelline vasculature morphology / MGI
- decreased liver weight / MGI
- pallor / MGI
- enhanced coordination / MGI
- decreased fetal size / MGI
- hematopoietic system phenotype / MGI
- abnormal hemoglobin content / MGI
- abnormal granulocyte differentiation / MGI
- abnormal monocyte differentiation / MGI
- abnormal placental labyrinth vasculature morphology / MGI
- decreased erythroid progenitor cell number / MGI
- postnatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI