- aortitis / MGI
- immune system phenotype / MGI
- hemorrhage / MGI
- premature death / MGI
- chronic inflammation / MGI
- artery stenosis / MGI
- skin inflammation / MGI
- psoriasis / MGI
- skin lesions / MGI
- abnormal epidermal layer morphology / MGI
- thick epidermis / MGI
- epidermal desquamation / MGI
- abnormal dermal layer morphology / MGI
- thick dermal layer / MGI
- parakeratosis / MGI
- abnormal keratinocyte physiology / MGI
- rheumatoid arthritis / MGI
- pathological neovascularization / MGI
B6.129P2(Cg)-Il1rntm1Nick/NickH
Status | Available to order |
EMMA ID | EM:02498 |
International strain name | B6.129P2(Cg)-Il1rntm1Nick/NickH |
Alternative name | C57BL/6 Il1rn |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Il1rntm1Nick |
Gene/Transgene symbol | Il1rn |
Information from provider
Provider | Martin Nicklin |
Provider affiliation | School of Medicine, University of Sheffield |
Genetic information | Inactivation of all isoforms of Il1rn by targeted replacement. Mutant locus contains plasmid and Neo marker. Strain lacks interleukin-1 receptor antagonist. |
Phenotypic information | Strain resistant to arthritis, arteritis and psoriasis (seen in BALB/c background) but highly susceptible to undefined "malaise" under conventional conditions. |
Breeding history | 129P2 chim. outbr. to MF1, inbred 4 gen., barrier rederived, backcrossed 4 gen. to BALB/cAnN then backcrossed to B6. |
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 |
Breeding at archiving centre | Males were archived by sperm freezing on arrival. No breeding was performed at the archiving centre. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Sterile multifocal osteomyelitis with periostitis and pustulosis / Orphanet_210115
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- psoriasis / MGI
- skin lesions / MGI
- abnormal epidermal layer morphology / MGI
- thick epidermis / MGI
- epidermal desquamation / MGI
- abnormal dermal layer morphology / MGI
- thick dermal layer / MGI
- decreased body weight / MGI
- postnatal growth retardation / MGI
- abnormal body temperature homeostasis / MGI
- hemorrhage / MGI
- reduced fertility / MGI
- premature death / MGI
- decreased susceptibility to bacterial infection / MGI
- abnormal CD4-positive, alpha beta T cell morphology / MGI
- abnormal T-helper 1 cell morphology / MGI
- abnormal T-helper 2 cell morphology / MGI
- chronic inflammation / MGI
- granulomatous inflammation / MGI
- abnormal immune system organ morphology / MGI
- parakeratosis / MGI
- abnormal keratinocyte physiology / MGI
- rheumatoid arthritis / MGI
- pathological neovascularization / MGI
- abnormal vascular wound healing / MGI
- skin inflammation / MGI
- increased acute inflammation / MGI
- decreased circulating cholesterol level / MGI
- immune system phenotype / MGI
- artery stenosis / MGI
- abnormal dendritic cell differentiation / MGI
- abnormal dendritic cell number / MGI
- decreased circulating interleukin-1 level / MGI
- increased circulating interleukin-6 level / MGI
- increased interleukin-17 secretion / MGI
- increased susceptibility to endotoxin shock / MGI
- aortitis / MGI
- abnormal circulating serum amyloid protein level / MGI
Literature references
- Elastic-vessel arteritis in interleukin-1 receptor antagonist-deficient mice involves effector Th1 cells and requires interleukin-1 receptor.;Shepherd Joanna, Nicklin Martin J H, ;2005;Circulation;111;3135-40; 15939811
- Stimulation of TLR2 and TLR4 differentially skews the balance of T cells in a mouse model of arthritis.;Abdollahi-Roodsaz Shahla, Joosten Leo A B, Koenders Marije I, Devesa Isabel, Roelofs Mieke F, Radstake Timothy R D J, Heuvelmans-Jacobs Marleen, Akira Shizuo, Nicklin Martin J H, Ribeiro-Dias Fátima, van den Berg Wim B, ;2008;The Journal of clinical investigation;118;205-16; 18060042
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