- abnormal spleen morphology / IMPC
- decreased prepulse inhibition / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased locomotor activity / IMPC
- impaired cued conditioning behavior / IMPC
- edema / IMPC
- male infertility / IMPC
- increased circulating creatinine level / IMPC
- increased freezing behavior / IMPC
- abnormal freezing behavior / IMPC
- decreased exploration in new environment / IMPC
- decreased fasting circulating glucose level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
C57BL/6N-Arid1btm1a(EUCOMM)Hmgu/Cnbc
Status | Available to order |
EMMA ID | EM:10411 |
Citation information | RRID:IMSR_EM:10411 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-Arid1btm1a(EUCOMM)Hmgu/Cnbc |
Alternative name | C57BL/6N-Arid1b |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Arid1btm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Arid1b |
Information from provider
Provider | Pedro Medina |
Provider affiliation | Pfizer - Junta de Andalucia - Universidad de Granada, Center for Genomics and Ontology Reseach (GenyO) |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0532_6_A11. |
Phenotypic information | Homozygous:Potential phenotyping data in the IMPC portalHeterozygous:See above |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Coffin-Siris syndrome / Orphanet_1465
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- muscle weakness / MGI
- decreased corpus callosum size / MGI
- abnormal dentate gyrus morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- decreased body size / MGI
- increased anxiety-related response / MGI
- increased grooming behavior / MGI
- abnormal vocalization / MGI
- postnatal growth retardation / MGI
- abnormal homeostasis / MGI
- hydroencephaly / MGI
- small heart / MGI
- decreased heart weight / MGI
- small kidney / MGI
- decreased kidney weight / MGI
- decreased circulating insulin-like growth factor I level / MGI
- behavior/neurological phenotype / MGI
- abnormal hypothalamus physiology / MGI
- thin cerebral cortex / MGI
- abnormal insulin-like growth factor I level / MGI
- decreased neuron number / MGI
- decreased birth body size / MGI
- decreased grip strength / MGI
- perinatal lethality, complete penetrance / MGI
- decreased dentate gyrus size / MGI
- abnormal response to social novelty / MGI
- decreased cerebral cortex cell number / MGI
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).