- right pulmonary isomerism / MGI
- abnormal autopod morphology / MGI
- abnormal liver morphology / MGI
- abnormal spleen morphology / MGI
- abnormal embryo implantation / MGI
- reduced fertility / MGI
- abnormal cardiovascular system morphology / MGI
- situs inversus / MGI
- abnormal heart atrium morphology / MGI
- left pulmonary isomerism / MGI
- right atrial isomerism / MGI
- abnormal inferior vena cava morphology / MGI
- left atrial isomerism / MGI
- increased physiological sensitivity to xenobiotic / MGI
- abnormal heart atrium auricular region morphology / MGI
- abnormal hepatic portal vein morphology / MGI
- abnormal motile primary cilium morphology / MGI
- heterotaxia / MGI
- absent nodal flow / MGI
STOCK Dnah11iv/H
Status | Available to order |
EMMA ID | EM:02531 |
Citation information | RRID:IMSR_EM:02531 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 Dnah11iv/H |
Alternative name | iv |
Strain type | Spontaneous |
Allele/Transgene symbol | Dnah11iv |
Gene/Transgene symbol | Dnah11 |
Information from provider
Provider | Katharine Hummel |
Provider affiliation | Medical Research Council |
Additional owner | For further information contact Martin Fray, FESA Manager. m.fray@har.mrc.ac.uk |
Genetic information | Homozygotes have randomised situs (sidedness). |
Phenotypic information | 50% of homozygotes have situs inversus totalis. |
Breeding history | Complex mixed background; inbred over more than 20 generations. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Primary ciliary dyskinesia / Orphanet_244
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal heart morphology / MGI
- heart right ventricle hypertrophy / MGI
- double outlet right ventricle / MGI
- abnormal mitral valve morphology / MGI
- abnormal intestine morphology / MGI
- hydronephrosis / MGI
- right pulmonary isomerism / MGI
- left-sided isomerism / MGI
- abnormal autopod morphology / MGI
- abnormal liver morphology / MGI
- dextrocardia / MGI
- mesocardia / MGI
- abnormal spleen morphology / MGI
- spleen hypoplasia / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- abnormal left-right axis patterning / MGI
- abnormal embryo implantation / MGI
- edema / MGI
- reduced fertility / MGI
- decreased litter size / MGI
- abnormal respiration / MGI
- perinatal lethality / MGI
- abnormal cardiovascular system morphology / MGI
- abnormal kidney morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal myocardial trabeculae morphology / MGI
- heart left ventricle hypertrophy / MGI
- micrognathia / MGI
- situs inversus / MGI
- abnormal heart atrium morphology / MGI
- left pulmonary isomerism / MGI
- accessory spleen / MGI
- decreased heart right ventricle size / MGI
- kidney cysts / MGI
- duplex kidney / MGI
- abnormal primitive node morphology / MGI
- abnormal motile primary cilium morphology / MGI
- heterotaxia / MGI
- interrupted aortic arch / MGI
- right aortic arch / MGI
- abnormal respiratory conducting tube morphology / MGI
- abnormal vertebral column morphology / MGI
- abnormal thoracic cavity morphology / MGI
- abnormal biliary tract morphology / MGI
- right atrial isomerism / MGI
- abnormal inferior vena cava morphology / MGI
- pulmonary valve stenosis / MGI
- left atrial isomerism / MGI
- polycystic kidney / MGI
- increased physiological sensitivity to xenobiotic / MGI
- abnormal motile primary cilium physiology / MGI
- ventricular septal defect / MGI
- ostium primum atrial septal defect / MGI
- atrioventricular septal defect / MGI
- complete atrioventricular septal defect / MGI
- muscular ventricular septal defect / MGI
- pulmonary artery hypoplasia / MGI
- vascular ring / MGI
- abnormal heart atrium auricular region morphology / MGI
- common atrioventricular valve / MGI
- abnormal hepatic portal vein morphology / MGI
- abnormal stomach position or orientation / MGI
- right-sided stomach / MGI
- abnormal lung lobe morphology / MGI
- abnormal respiratory motile cilium physiology / MGI
- abdominal situs inversus / MGI
- abdominal situs ambiguus / MGI
- situs inversus totalis / MGI
- situs inversus with levocardia / MGI
- superior-inferior ventricles / MGI
- biventricular, discordant atrioventricular connection / MGI
- biventricular, ambiguous atrioventricular connection / MGI
- immotile respiratory cilia / MGI
- d-loop transposition of the great arteries / MGI
- double outlet right ventricle, ventricular defect committed to aorta / MGI
- dual inferior vena cava / MGI
- isolation of the left subclavian artery / MGI
- absent nodal flow / MGI
Literature references
- Situs Viscerum Inversus;Hummel KP, Chapman D;1959;Mouse News Lett.;14;21; 9353118
- Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice.;Supp D M, Witte D P, Potter S S, Brueckner M, ;1997;Nature;389;963-6;
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