- decreased hematocrit / IMPC
- abnormal response to new environment / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating bilirubin level / IMPC
- abnormal retina blood vessel pattern / IMPC
C57BL/6NTac-Prkab1tm1a(KOMP)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:13978 |
International strain name | C57BL/6NTac-Prkab1tm1a(KOMP)Wtsi/WtsiPh |
Alternative name | EPD0033_3_C09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Prkab1tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Prkab1 |
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 EPD0033_3_C09. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased fasting circulating glucose level / IMPC
- decreased hematocrit / IMPC
- increased memory-marker gamma-delta T cell number / IMPC
- enlarged spleen / IMPC
- decreased grip strength / IMPC
- increased glycosylated hemoglobin level / IMPC
- decreased mean corpuscular volume / IMPC
- decreased hemoglobin content / IMPC
- decreased total retina thickness / IMPC
- hyperplasia / IMPC
- increased spleen weight / IMPC
- absent pinna reflex / IMPC
- enlarged heart / IMPC
- abnormal spleen morphology / IMPC
- impaired glucose tolerance / IMPC
- enlarged testis / IMPC
- increased memory-marker CD4-negative NK T cell number / IMPC
- abnormal epididymis morphology / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- decreased circulating cholesterol level / IMPC
- increased red blood cell distribution width / IMPC
- abnormal thymus morphology / IMPC
- decreased Ly6C-positive mature NK cell number / IMPC
- abnormal response to new environment / IMPC
- increased fasting circulating glucose level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- increased heart weight / IMPC
- decreased circulating phosphate level / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal retina blood vessel morphology / IMPC
- decreased circulating amylase level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- fibro-osseous lesion / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- shortened RR interval / IMPC
- enlarged epididymis / IMPC
- increased circulating bilirubin level / IMPC
- cataract / IMPC
- increased neutrophil cell number / IMPC
- abnormal heart left ventricle morphology / IMPC
- abnormal heart morphology / IMPC
- abnormal freezing behavior / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
- decreased circulating LDL cholesterol level / IMPC
- abnormal lens morphology / IMPC
- enlarged kidney / IMPC
- increased circulating alkaline phosphatase level / IMPC
- impaired contextual conditioning behavior / IMPC
- decreased circulating iron level / IMPC
- abnormal kidney morphology / IMPC
- no spontaneous movement / IMPC
- decreased lymphocyte cell number / IMPC
- abnormal retina vasculature morphology / IMPC
- increased mean platelet volume / IMPC
- enlarged thymus / IMPC
- decreased body weight / IMPC
- decreased circulating chloride level / IMPC
- increased lung compliance / IMPC
- abnormal retina blood vessel pattern / IMPC
- decreased kidney weight / IMPC
- decreased bone mineral density / IMPC
- decreased lung elastance / IMPC
- increased heart rate / IMPC
- decreased bone mineral content / IMPC
- abnormal testis morphology / IMPC
- anophthalmia / IMPC
- increased circulating alanine transaminase level / IMPC
MGI phenotypes (allele matching)
- decreased hematocrit / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- increased circulating bilirubin level / MGI
- decreased mean corpuscular hemoglobin / MGI
- abnormal inferior vena cava morphology / MGI
- decreased circulating magnesium level / MGI
- abnormal ductus venosus morphology / MGI
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- extramedullary hematopoiesis / MGI
- abnormal erythropoiesis / MGI
- echinocytosis / MGI
- schistocytosis / MGI
- enlarged spleen / MGI
- tremors / MGI
- decreased brain size / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal dentate gyrus morphology / MGI
- abnormal cerebellum morphology / MGI
- absent cerebellar granule layer / MGI
- abnormal myelination / MGI
- decreased body weight / MGI
- abnormal optic nerve morphology / MGI
- ataxia / MGI
- abnormal lipid level / MGI
- hemolytic anemia / MGI
- seizures / MGI
- no abnormal phenotype detected / MGI
- abnormal astrocyte morphology / MGI
- decreased susceptibility to hepatic steatosis / MGI
- abnormal bone marrow morphology / MGI
- abnormal erythrocyte morphology / MGI
- increased mean platelet volume / MGI
- reticulocytosis / MGI
- anisocytosis / MGI
- decreased circulating insulin level / MGI
- microcytic anemia / MGI
- microcytosis / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- increased insulin sensitivity / MGI
- increased erythroid progenitor cell number / MGI
- loss of hippocampal neurons / MGI
- astrocytosis / MGI
- abnormal erythrocyte osmotic lysis / MGI
- decreased circulating iron level / MGI
- abnormal neuronal precursor proliferation / MGI
- increased spleen weight / MGI
- increased circulating bilirubin level / MGI
- renal/urinary system phenotype / MGI
- homeostasis/metabolism phenotype / MGI
- abnormal axon morphology / MGI
- decreased mean corpuscular hemoglobin / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- decreased susceptibility to diet-induced obesity / MGI
- decreased circulating leptin level / MGI
- abnormal inferior vena cava morphology / MGI
- optic nerve hypoplasia / MGI
- brain vacuoles / MGI
- abnormal dendrite morphology / MGI
- increased spleen red pulp amount / MGI
- slow postnatal weight gain / MGI
- decreased circulating interleukin-6 level / MGI
- increased spleen iron level / MGI
- decreased cerebellar granule cell number / MGI
- decreased neuron number / MGI
- decreased epididymal fat pad weight / MGI
- decreased liver triglyceride level / MGI
- decreased oligodendrocyte number / MGI
- abnormal neuron differentiation / MGI
- increased red blood cell distribution width / MGI
- stomatocytosis / MGI
- abnormal hepatocyte physiology / MGI
- decreased circulating magnesium level / MGI
- acanthocytosis / MGI
- postnatal lethality, complete penetrance / MGI
- increased erythroblast number / MGI
- increased circulating erythropoietin level / MGI
- increased circulating ferritin level / MGI
- abnormal reticulocyte cell number / MGI
- decreased food intake / MGI
- abnormal ductus venosus morphology / MGI
- cerebellum atrophy / 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
- Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse.;DiTommaso Tia, Jones Lynelle K, Cottle Denny L, null null, Gerdin Anna-Karin, Vancollie Valerie E, Watt Fiona M, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, Sundberg John P, White Jacqueline K, Smyth Ian M, ;2014;PLoS genetics;10;e1004705; 25340873
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