- hyperactivity / IMPC
- abnormal auditory brainstem response / IMPC
- increased aggression / IMPC
- abnormal vocalization / IMPC
- decreased bone mineral density / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal contextual conditioning behavior / IMPC
- increased circulating creatinine level / IMPC
- increased exploration in new environment / IMPC
- increased lean body mass / IMPC
- abnormal spleen morphology / IMPC
- increased vertical activity / IMPC
- abnormal locomotor behavior / IMPC
- abnormal cued conditioning behavior / IMPC
C57BL/6N-Ptchd1em1(IMPC)Ics/Ics
Status | Available to order |
EMMA ID | EM:15794 |
Citation information | RRID:IMSR_EM:15794 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-Ptchd1em1(IMPC)Ics/Ics |
Alternative name | Ptchd1em1(IMPC)Ics |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Ptchd1em1(IMPC)Ics |
Gene/Transgene symbol | Ptchd1 |
Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This allele was generated at the Institute Clinique de la Souris by electroporating Cas9 protein, a crRNA (GTTGATTGATTGCAGATAGT)/tracRNA and a single stranded donor DNA, which resulted in the p.Y213C mutation of Ptchd1 exon 2 (ENSMUSE00000252591; GRCm39). A NspI diagnostic restriction site is associated to the mutation to facilitate genotyping. This line is cryopreserved. |
Phenotypic information | Homozygous:NAHeterozygous:Viable, no obvious phenotype |
Breeding history | This line was generated on a pure C57BL/6N genetic background. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).