MGI phenotypes (allele matching)
- decreased rhombomere 3 size / MGI
STOCK Egr2tm3Pch Tg(CD2-icre)4Kio/H
| Status | Available to order |
| EMMA ID | EM:04482 |
| Citation information | RRID:IMSR_EM:04482 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 Egr2tm3Pch Tg(CD2-icre)4Kio/H |
| Alternative name | Egr-2-cKO |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Egr2tm3Pch, Tg(CD2-icre)4Kio |
| Gene/Transgene symbol | Egr2, Tg(CD2-icre)4Kio |
Information from provider
| Provider | Ping Wang |
| Provider affiliation | Institute of Cell and Molecular Science, Bart and London School of Medicien and Dentistry |
| Genetic information | Egr2 loxP and CD2-cre. |
| Phenotypic information | Spontaneous autoimmune diseases start at late age (12 months). |
| Breeding history | Inbred |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
| Animals used for archiving | homozygous C57BL/6 x CBA males |
| Breeding at archiving centre | Males were archived upon arrival. No breeding was performed at the archiving centre. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Dejerine-Sottas syndrome / Orphanet_64748
- Charcot-Marie-Tooth disease type 1D / Orphanet_101084
- Charcot-Marie-Tooth disease type 4E / Orphanet_99951
MGI phenotypes (gene matching)
- abnormal mandible morphology / MGI
- tremors / MGI
- weakness / MGI
- paralysis / MGI
- hindlimb paralysis / MGI
- abnormal myelination / MGI
- abnormal rhombomere morphology / MGI
- abnormal motor neuron morphology / MGI
- abnormal spinal cord morphology / MGI
- abnormal neuromuscular synapse morphology / MGI
- abnormal cranial nerve morphology / MGI
- abnormal trigeminal nerve morphology / MGI
- abnormal abducens nerve morphology / MGI
- abnormal facial nerve morphology / MGI
- abnormal glossopharyngeal nerve morphology / MGI
- abnormal vagus nerve morphology / MGI
- abnormal cranial ganglia morphology / MGI
- abnormal geniculate ganglion morphology / MGI
- abnormal trigeminal ganglion morphology / MGI
- abnormal glossopharyngeal ganglion morphology / MGI
- abnormal vagus ganglion morphology / MGI
- abnormal Schwann cell morphology / MGI
- decreased body weight / MGI
- weight loss / MGI
- decreased body size / MGI
- delayed eyelid opening / MGI
- hypoactivity / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- impaired limb coordination / MGI
- postnatal growth retardation / MGI
- respiratory distress / MGI
- abnormal motor capabilities/coordination/movement / MGI
- abnormal skeleton development / MGI
- abnormal neural tube morphology / MGI
- abnormal sciatic nerve morphology / MGI
- abnormal aortic valve morphology / MGI
- abnormal somatic nervous system morphology / MGI
- short tibia / MGI
- abnormal cochlear ganglion morphology / MGI
- abnormal bone mineralization / MGI
- no phenotypic analysis / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- short femur / MGI
- decreased width of hypertrophic chondrocyte zone / MGI
- abnormal long bone morphology / MGI
- abnormal bone structure / MGI
- short radius / MGI
- fusion of glossopharyngeal and vagus nerve / MGI
- decreased length of long bones / MGI
- increased pulmonary respiratory rate / MGI
- abnormal neuronal migration / MGI
- abnormal hindbrain development / MGI
- decreased diameter of long bones / MGI
- decreased diameter of femur / MGI
- decreased diameter of radius / MGI
- decreased diameter of tibia / MGI
- decreased nerve conduction velocity / MGI
- enlarged aortic valve / MGI
- thick aortic valve cusps / MGI
- thick pulmonary valve cusps / MGI
- integument phenotype / MGI
- lethality at weaning, complete penetrance / MGI
- postnatal lethality, complete penetrance / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- increased Schwann cell proliferation / MGI
- decreased rhombomere 3 size / MGI
- absent rhombomere 3 / MGI
- decreased rhombomere 5 size / MGI
- absent rhombomere 5 / MGI
- decreased rhombomere 6 size / MGI
Literature references
- Early growth response gene 2 (Egr-2) controls the self-tolerance of T cells and prevents the development of lupuslike autoimmune disease.;Zhu Bo, Symonds Alistair L J, Martin Joanne E, Kioussis Dimitris, Wraith David C, Li Suling, Wang Ping, ;2008;The Journal of experimental medicine;205;2295-307; 18779345