C57BL/6N-Atm1Brd Gas2l2tm1a(KOMP)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:11597 |
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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