- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Dhx35tm1b(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:14263 |
International strain name | C57BL/6N-Dhx35tm1b(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0546_4_C06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Dhx35tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Dhx35 |
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 EUCOMM ES clone EPD0546_4_C06. 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 EUCOMM final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
MGI phenotypes (allele matching)
- abnormal vertebrae morphology / MGI
- scoliosis / MGI
- double outlet right ventricle / MGI
- short snout / MGI
- absent mammary gland / MGI
- persistent truncus arteriosis / MGI
- absent olfactory bulb / MGI
- right aortic arch / MGI
- abnormal adenohypophysis morphology / MGI
- abnormal optic cup morphology / MGI
- basisphenoid bone foramen / MGI
- holoprosencephaly / MGI
- abnormal brain internal capsule morphology / MGI
- thoracoschisis / MGI
- perimembraneous ventricular septal defect / MGI
- muscular ventricular septal defect / MGI
- common truncal valve / MGI
- abnormal basilar artery morphology / MGI
- abnormal hypoglossal nerve topology / MGI
- retro-esophageal left subclavian artery / MGI
- absent connection between subcutaneous lymph vessels and lymph sac / MGI
- symmetric azygos veins / MGI
- double lumen aortic arch / MGI
- abnormal vertebral artery origin / MGI
MGI phenotypes (gene matching)
- abnormal vertebrae morphology / MGI
- scoliosis / MGI
- double outlet right ventricle / MGI
- short snout / MGI
- absent mammary gland / MGI
- persistent truncus arteriosis / MGI
- absent olfactory bulb / MGI
- right aortic arch / MGI
- abnormal adenohypophysis morphology / MGI
- abnormal optic cup morphology / MGI
- basisphenoid bone foramen / MGI
- holoprosencephaly / MGI
- abnormal brain internal capsule morphology / MGI
- thoracoschisis / MGI
- perimembraneous ventricular septal defect / MGI
- muscular ventricular septal defect / MGI
- common truncal valve / MGI
- abnormal basilar artery morphology / MGI
- abnormal hypoglossal nerve topology / MGI
- retro-esophageal left subclavian artery / MGI
- absent connection between subcutaneous lymph vessels and lymph sac / MGI
- symmetric azygos veins / MGI
- double lumen aortic arch / MGI
- abnormal vertebral artery origin / MGI
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