Apbb2 | amyloid beta precursor protein binding family B member 2
Physiological systems
23 / 24 physiological systems tested
9 Significantly impacted by the knock-out
Homeostasis/metabolism Integument Embryo Growth/size/body region Nervous system Vision/eye Respiratory system Cardiovascular system Mortality/aging
14 No significant impact
1 Not tested
Gene metrics:8Significant phenotypes
0Associated diseases
Expression examined in:73Adult tissues
81Embryo tissues
spina bifida | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | homozygote | E15.5 | N/A * | ||
hemorrhage | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | homozygote | E15.5 | N/A * | ||
hemorrhage | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | E15.5 | N/A * | ||
abnormal eye morphology | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | Early adult | N/A * | ||
spina bifida | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | E15.5 | N/A * | ||
preweaning lethality, incomplete penetrance | 2 supporting datasets | Apbb2tm1.1(KOMP)Vlcg | homozygote | Early adult | N/A * | ||
increased circulating aspartate transaminase level | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | Early adult | 2.03x10-7 | ||
increased lung weight | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | Early adult | 1.71x10-5 | ||
increased circulating alanine transaminase level | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | Early adult | 2.48x10-8 | ||
abnormal skin morphology | 1 supporting dataset | Apbb2tm1.1(KOMP)Vlcg | heterozygote | Early adult | N/A * |
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External links
No external links available for Apbb2.
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Apbb2tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | | ES Cell mouse |
Apbb2tm1.1(KOMP)Vlcg | Reporter-tagged deletion allele (post Cre, with no selection cassette) | | mouse |
Apbb2tm448183(L1L2_GT1_LF2A_LacZ_BetactP_neo) | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector |