- 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 |
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 |
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
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