- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Anks6tm1b(KOMP)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:14337 |
International strain name | C57BL/6N-Anks6tm1b(KOMP)Wtsi/WtsiIeg |
Alternative name | EPD0109_5_D01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Anks6tm1b(KOMP)Wtsi |
Gene/Transgene symbol | Anks6 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0109_5_D01. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele using a cell permeable HTN-Cre as described in doi:10.1007/s11248-013-9764-x. Click here for more information on KOMP final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Infantile nephronophthisis / Orphanet_93591
- Juvenile nephronophthisis / Orphanet_93592
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
MGI phenotypes (allele matching)
- abnormal interatrial septum morphology / MGI
- abnormal lung morphology / MGI
- abnormal aortic valve morphology / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- transposition of great arteries / MGI
- fetal growth retardation / MGI
- common atrium / MGI
- perimembraneous ventricular septal defect / MGI
- anomalous pulmonary venous connection / MGI
- common atrioventricular valve / MGI
- lung situs inversus / MGI
- abdominal situs inversus / MGI
- dual inferior vena cava / MGI
- absent ductus venosus valve / MGI
- abnormal coronary sinus connection / MGI
- symmetric azygos veins / MGI
MGI phenotypes (gene matching)
- overriding aortic valve / MGI
- abnormal interatrial septum morphology / MGI
- abnormal liver morphology / MGI
- dextrocardia / MGI
- abnormal lung morphology / MGI
- abnormal aortic valve morphology / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- transposition of great arteries / MGI
- heterotaxia / MGI
- fetal growth retardation / MGI
- right atrial isomerism / MGI
- abnormal inferior vena cava morphology / MGI
- ventricular septal defect / MGI
- common atrium / MGI
- atrioventricular septal defect / MGI
- perimembraneous ventricular septal defect / MGI
- anomalous pulmonary venous connection / MGI
- common atrioventricular valve / MGI
- lung situs inversus / MGI
- abdominal situs inversus / MGI
- dual inferior vena cava / MGI
- absent ductus venosus valve / MGI
- abnormal coronary sinus connection / MGI
- symmetric azygos veins / MGI
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