- preweaning lethality, incomplete penetrance / IMPC
B6Brd;B6N-Tyrc-Brd Slx4tm1a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:05091 |
International strain name | B6Brd;B6N-Tyrc-Brd Slx4tm1a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0028_7_A08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slx4tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Slx4 |
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 EPD0028_7_A08. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Fanconi anemia / Orphanet_84
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, incomplete penetrance / IMPC
MGI phenotypes (allele matching)
- decreased leukocyte cell number / MGI
- abnormal cranium morphology / MGI
- enlarged cranium / MGI
- domed cranium / MGI
- abnormal cerebral cortex morphology / MGI
- dilated lateral ventricles / MGI
- abnormal third ventricle morphology / MGI
- obstructive hydrocephaly / MGI
- absent mature ovarian follicles / MGI
- absent corpus luteum / MGI
- abnormal spermatogenesis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- abnormal cornea morphology / MGI
- corneal opacity / MGI
- abnormal pupil morphology / MGI
- abnormal iris morphology / MGI
- absent optic nerve / MGI
- postnatal growth retardation / MGI
- hydroencephaly / MGI
- reduced male fertility / MGI
- reduced female fertility / MGI
- decreased litter size / MGI
- abnormal eye morphology / MGI
- abnormal tooth morphology / MGI
- abnormal lymphopoiesis / MGI
- oligozoospermia / MGI
- abnormal retinal vasculature morphology / MGI
- increased erythrocyte cell number / MGI
- thrombocytopenia / MGI
- nervous system phenotype / MGI
- abnormal eyelid aperture / MGI
- abnormal spine curvature / MGI
- vertebral fusion / MGI
- absent oocytes / MGI
- azoospermia / MGI
- impaired glucose tolerance / MGI
- increased circulating glucose level / MGI
- thin cerebral cortex / MGI
- early cellular replicative senescence / MGI
- abnormal male germ cell apoptosis / MGI
- abnormal primordial germ cell morphology / MGI
- decreased common myeloid progenitor cell number / MGI
- chromosomal instability / MGI
- increased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced cell death / MGI
- increased caudal vertebrae number / MGI
- perinatal lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- abnormal eye size / MGI
MGI phenotypes (gene matching)
- decreased leukocyte cell number / MGI
- abnormal cranium morphology / MGI
- enlarged cranium / MGI
- domed cranium / MGI
- abnormal cerebral cortex morphology / MGI
- dilated lateral ventricles / MGI
- abnormal third ventricle morphology / MGI
- obstructive hydrocephaly / MGI
- absent mature ovarian follicles / MGI
- absent corpus luteum / MGI
- small testis / MGI
- abnormal spermatogenesis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- abnormal cornea morphology / MGI
- corneal opacity / MGI
- abnormal pupil morphology / MGI
- abnormal iris morphology / MGI
- absent optic nerve / MGI
- postnatal growth retardation / MGI
- hydroencephaly / MGI
- reduced male fertility / MGI
- reduced female fertility / MGI
- decreased litter size / MGI
- abnormal eye morphology / MGI
- abnormal tooth morphology / MGI
- abnormal lymphopoiesis / MGI
- oligozoospermia / MGI
- abnormal eye size / MGI
- abnormal retinal vasculature morphology / MGI
- no phenotypic analysis / MGI
- increased erythrocyte cell number / MGI
- thrombocytopenia / MGI
- nervous system phenotype / MGI
- abnormal eyelid aperture / MGI
- induced chromosome breakage / MGI
- abnormal spine curvature / MGI
- vertebral fusion / MGI
- absent oocytes / MGI
- azoospermia / MGI
- impaired glucose tolerance / MGI
- increased circulating glucose level / MGI
- thin cerebral cortex / MGI
- early cellular replicative senescence / MGI
- abnormal DNA repair / MGI
- abnormal male germ cell apoptosis / MGI
- abnormal primordial germ cell morphology / MGI
- decreased common myeloid progenitor cell number / MGI
- chromosomal instability / MGI
- increased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced cell death / MGI
- increased caudal vertebrae number / MGI
- abnormal telomere morphology / MGI
- perinatal lethality, incomplete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- embryonic lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / 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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