Symbol Name ID |
Abhd5
abhydrolase domain containing 5 MGI:1914719 |
Darker colors indicate more annotations |
Human Phenotypes | Gangrene |
Disease(s) Associated with ABHD5 | |
autosomal recessive congenital ichthyosis 1 |
Mouse Phenotypes | increased cardiac muscle cell glucose uptake |
abnormal keratinocyte differentiation |
decreased fatty acid oxidation |
oxidative stress |
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Availability | Mouse Genotype | ||||
Abhd5tm1.1Rze/Abhd5tm1.1Rze | |||||
Abhd5tm1.1Lqyu/Abhd5tm1.1Lqyu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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Abhd5tm1Rze/Abhd5tm1Rze Tg(Ckmm-cre)5Khn/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 09/03/2024 MGI 6.24 |
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