C57BL/6N-Atm1Brd Gas2l2tm1a(KOMP)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:11597 |
Citation information | RRID:IMSR_EM:11597 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 | C57BL/6N-Atm1Brd Gas2l2tm1a(KOMP)Wtsi/WtsiOulu |
Alternative name | EPD0626_4_G11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Gas2l2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Gas2l2 |
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 EPD0626_4_G11. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Primary ciliary dyskinesia / Orphanet_244
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- abnormal basisphenoid bone morphology / MGI
- abnormal vertebral body morphology / MGI
- abnormal snout morphology / MGI
- enlarged liver sinusoidal spaces / MGI
- absent salivary gland / MGI
- abnormal forebrain morphology / MGI
- abnormal midbrain morphology / MGI
- incomplete rostral neuropore closure / MGI
- fused dorsal root ganglion / MGI
- anophthalmia / MGI
- aphakia / MGI
- biliary cyst / MGI
- abnormal auditory tube / MGI
- dilated ureter / MGI
- abnormal eye muscle morphology / MGI
- abnormal optic stalk morphology / MGI
- absent vertebral arch / MGI
- fusion of vertebral arches / MGI
- absent stapedial artery / MGI
- abnormal Meckel's cartilage morphology / MGI
- oral atresia / MGI
- absent tongue / MGI
- perimembraneous ventricular septal defect / MGI
- absent optic cup / MGI
- absent segment of anterior cerebral artery / MGI
- abnormal Mullerian duct topology / MGI
- trigeminal neuroma / MGI
- abnormal ductus venosus valve morphology / MGI
- abnormal thymus topology / MGI
- abnormal left vena cava superior connection / MGI
- abnormal external carotid artery origin / MGI
- abnormal vertebral artery topology / MGI
- embryo tumor / MGI
MGI phenotypes (gene matching)
- abnormal basisphenoid bone morphology / MGI
- abnormal vertebral body morphology / MGI
- abnormal snout morphology / MGI
- enlarged liver sinusoidal spaces / MGI
- absent salivary gland / MGI
- abnormal forebrain morphology / MGI
- abnormal midbrain morphology / MGI
- incomplete rostral neuropore closure / MGI
- fused dorsal root ganglion / MGI
- anophthalmia / MGI
- no abnormal phenotype detected / MGI
- aphakia / MGI
- biliary cyst / MGI
- abnormal auditory tube / MGI
- dilated ureter / MGI
- abnormal eye muscle morphology / MGI
- abnormal optic stalk morphology / MGI
- absent vertebral arch / MGI
- fusion of vertebral arches / MGI
- absent stapedial artery / MGI
- abnormal Meckel's cartilage morphology / MGI
- oral atresia / MGI
- absent tongue / MGI
- perimembraneous ventricular septal defect / MGI
- absent optic cup / MGI
- absent segment of anterior cerebral artery / MGI
- abnormal Mullerian duct topology / MGI
- trigeminal neuroma / MGI
- abnormal ductus venosus valve morphology / MGI
- abnormal thymus topology / MGI
- abnormal left vena cava superior connection / MGI
- abnormal external carotid artery origin / MGI
- abnormal vertebral artery topology / MGI
- embryo tumor / MGI
- abnormal middle cerebral artery origin / MGI
- abnormal ophthalmic artery origin / MGI
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