Symbol Name ID |
Abhd5
abhydrolase domain containing 5 MGI:1914719 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal granulocyte morphology |
Chronic otitis media |
Erythroderma |
Sepsis |
Recurrent respiratory infections |
Disease(s) Associated with ABHD5 | |||||
autosomal recessive congenital ichthyosis 1 | |||||
Chanarin-Dorfman syndrome |
Mouse Phenotypes | abnormal granulocyte morphology |
liver inflammation |
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Availability | Mouse Genotype | ||
Abhd5tm1.1Rze/Abhd5tm1.1Rze | |||
Abhd5tm1.1Lqyu/Abhd5tm1.1Lqyu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (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 04/23/2024 MGI 6.23 |
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