- decreased hematocrit / IMPC
- abnormal cranium morphology / IMPC
- abnormal maxilla morphology / IMPC
- decreased body length / IMPC
- decreased body weight / IMPC
- abnormal cornea morphology / IMPC
- corneal opacity / IMPC
- abnormal pupil morphology / IMPC
- abnormal iris morphology / IMPC
- abnormal eye pigmentation / IMPC
- abnormal eye morphology / IMPC
- abnormal tooth morphology / IMPC
- abnormal eye size / IMPC
- decreased hemoglobin content / IMPC
- abnormal eyelid aperture / IMPC
- decreased lean body mass / IMPC
- vertebral fusion / IMPC
- eyelids fail to open / IMPC
- corneal vascularization / IMPC
- increased circulating potassium level / IMPC
- increased circulating creatine kinase level / IMPC
- increased circulating magnesium level / IMPC
- decreased bone mineral content / IMPC
- preweaning lethality, incomplete penetrance / IMPC
B6Brd;B6N-Tyrc-Brd Kat14tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12068 |
International strain name | B6Brd;B6N-Tyrc-Brd Kat14tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0025_4_B07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Kat14tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Kat14 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0025_4_B07. 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 |
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Information from EMMA
Archiving centre | Wellcome Trust Sanger Institute, Hinxton, United Kingdom |
Animals used for archiving | homozygous C57BL/6J-Tyr |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal cornea morphology / IMPC
- decreased body weight / IMPC
- increased circulating magnesium level / IMPC
- abnormal eye morphology / IMPC
- increased circulating potassium level / IMPC
- decreased body length / IMPC
- abnormal iris morphology / IMPC
- corneal opacity / IMPC
- abnormal maxilla morphology / IMPC
- decreased hemoglobin content / IMPC
- abnormal eyelid aperture / IMPC
- increased circulating creatine kinase level / IMPC
- corneal vascularization / IMPC
- decreased hematocrit / IMPC
- abnormal tooth morphology / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal eye size / IMPC
- decreased bone mineral content / IMPC
- decreased lean body mass / IMPC
- abnormal cranium morphology / IMPC
- abnormal pupil morphology / IMPC
- eyelids fail to open / IMPC
- abnormal eye pigmentation / IMPC
- vertebral fusion / IMPC
MGI phenotypes (allele matching)
- vision/eye phenotype / MGI
- corneal opacity / MGI
- preweaning lethality, incomplete penetrance / MGI
- scoliosis / MGI
- abnormal cranium morphology / MGI
- abnormal maxilla morphology / MGI
- decreased body length / MGI
- abnormal eye development / MGI
- abnormal cornea morphology / MGI
- abnormal tooth morphology / MGI
- decreased susceptibility to bacterial infection / MGI
- abnormal eye size / MGI
- opacity of vitreous body / MGI
- decreased lean body mass / MGI
- abnormal spine curvature / MGI
- vertebral fusion / MGI
- fusion of vertebral arches / MGI
- eyelids fail to open / MGI
- abnormal zygomatic bone morphology / MGI
- abnormal corneal stroma morphology / MGI
- corneal vascularization / MGI
- lethality, incomplete penetrance / MGI
- abnormal eye pigmentation / MGI
- abnormal behavior / MGI
MGI phenotypes (gene matching)
- scoliosis / MGI
- abnormal cranium morphology / MGI
- abnormal maxilla morphology / MGI
- decreased body length / MGI
- abnormal eye development / MGI
- abnormal cornea morphology / MGI
- corneal opacity / MGI
- abnormal eye pigmentation / MGI
- decreased embryo size / MGI
- abnormal tooth morphology / MGI
- decreased susceptibility to bacterial infection / MGI
- abnormal eye size / MGI
- opacity of vitreous body / MGI
- abnormal cell cycle / MGI
- decreased lean body mass / MGI
- abnormal spine curvature / MGI
- vertebral fusion / MGI
- fusion of vertebral arches / MGI
- abnormal behavior / MGI
- eyelids fail to open / MGI
- abnormal zygomatic bone morphology / MGI
- abnormal corneal stroma morphology / MGI
- vision/eye phenotype / MGI
- corneal vascularization / MGI
- increased apoptosis / MGI
- lethality, incomplete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- increased embryonic neuroepithelium apoptosis / MGI
Literature references
- Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131
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