Symbol Name ID |
Asah1
N-acylsphingosine amidohydrolase 1 MGI:1277124 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatosplenomegaly |
Hepatomegaly |
Failure to thrive |
Disease(s) Associated with ASAH1 | ||||
Farber lipogranulomatosis | ||||
spinal muscular atrophy with progressive myoclonic epilepsy |
Mouse Phenotypes | weight loss |
cachexia |
postnatal growth retardation |
enlarged spleen |
increased spleen weight |
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Availability | Mouse Genotype | |||||
Asah1tm1.2Geno/Asah1tm1.2Geno | ||||||
Asah1tm1Medin/Asah1tm1Medin |
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 03/19/2024 MGI 6.23 |
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