- hypoplasia / IMPC
- mydriasis / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal sternum morphology / IMPC
- small heart / IMPC
- abnormal lung morphology / IMPC
- microphthalmia / IMPC
- abnormal testis morphology / IMPC
- abnormal seminal vesicle morphology / IMPC
- enlarged lymph nodes / IMPC
- small kidney / IMPC
- abnormal skin morphology / IMPC
- enlarged prostate gland / IMPC
- increased red blood cell distribution width / IMPC
- abnormal liver morphology / IMPC
B6.CAnNCrl(C3H)-Dync1li1m1Emcf/H
| Status | Available to order |
| EMMA ID | EM:04327 |
| Citation information | RRID:IMSR_EM:04327 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 | B6.CAnNCrl(C3H)-Dync1li1m1Emcf/H |
| Alternative name | Dync1li N235Y Cytoplasmic dynein light intermediate chain 1 N235Y mutation |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Dync1li1m1Emcf |
| Gene/Transgene symbol | Dync1li1 |
Information from provider
| Provider | Elizabeth Fisher |
| Provider affiliation | Neurodegenerative Disease, UCL Institute of Neurology |
| Additional owner | This mutant originally came from the Harwell- GSK ENU mutagenesis screen, number EMRCD/12.2b. |
| Genetic information | Carries and ENU induced point mutation in exon 5, a A to T change at bp 754 causing an asparagine to tyrosine change at residue 235. |
| Phenotypic information | Mouse not completely assessed but so far homozygotes have behavioural and neurological changes. |
| Breeding history | Mouse was sent from the ENU program at Harwell, thus first generation were (C3H/HeH x BALB/cAnN)F1. Backcrossed to C57BL/6J from then on. Mice submitted are at N6 backcrossed to C57BL/6J. |
| 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/6J males |
| Breeding at archiving centre | No breeding was performed at the archiving centre. Imported males were believed to be homozygous, backcross 6 to C57BL/6J. |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- increased anxiety-related response / MGI
- abnormal gait / MGI
- decreased exploration in new environment / MGI
- abnormal lysosome physiology / MGI
- nervous system phenotype / MGI
- increased defecation amount / MGI
- behavior/neurological phenotype / MGI
- abnormal action potential / MGI
- abnormal neuronal migration / MGI
- abnormal dendrite morphology / MGI
- increased grip strength / MGI
MGI phenotypes (gene matching)
- increased anxiety-related response / MGI
- abnormal gait / MGI
- decreased exploration in new environment / MGI
- abnormal lysosome physiology / MGI
- nervous system phenotype / MGI
- increased defecation amount / MGI
- behavior/neurological phenotype / MGI
- abnormal action potential / MGI
- abnormal neuronal migration / MGI
- abnormal dendrite morphology / MGI
- increased grip strength / MGI
Literature references
- Behavioral and other phenotypes in a cytoplasmic Dynein light intermediate chain 1 mutant mouse.;Banks Gareth T, Haas Matilda A, Line Samantha, Shepherd Hazel L, Alqatari Mona, Stewart Sammy, Rishal Ida, Philpott Amelia, Kalmar Bernadett, Kuta Anna, Groves Michael, Parkinson Nicholas, Acevedo-Arozena Abraham, Brandner Sebastian, Bannerman David, Greensmith Linda, Hafezparast Majid, Koltzenburg Martin, Deacon Robert, Fainzilber Mike, Fisher Elizabeth M C, ;2011;The Journal of neuroscience : the official journal of the Society for Neuroscience;31;5483-94; 21471385
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