- abnormal iris morphology / IMPC
- abnormal locomotor activation / IMPC
- abnormal pupil morphology / IMPC
- increased circulating alanine transaminase level / IMPC
- abnormal lens morphology / IMPC
- increased B cell number / IMPC
- decreased T cell number / IMPC
- abnormal eye morphology / IMPC
- cataract / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- increased startle reflex / IMPC
B6J.129S2-Nr1d2tm1.1Ics/Ics
Status | Available to order |
EMMA ID | EM:12932 |
International strain name | B6J.129S2-Nr1d2tm1.1Ics/Ics |
Alternative name | RevErbb CM |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Nr1d2tm1.1Ics |
Gene/Transgene symbol | Nr1d2 |
Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Phenotypic information | Homozygous:NAHeterozygous:NA |
Breeding history | 6 backcross generations |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
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)
MGI phenotypes (gene matching)
- abnormal heart morphology / MGI
- increased anxiety-related response / MGI
- no abnormal phenotype detected / MGI
- no phenotypic analysis / MGI
- impaired behavioral response to xenobiotic / MGI
- ostium primum atrial septal defect / MGI
- atrioventricular septal defect / MGI
- inlet ventricular septal defect / MGI
- common atrioventricular valve / MGI
- neonatal lethality, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
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