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Symbol
Name
ID
Asah1
N-acylsphingosine amidohydrolase 1
MGI:1277124
Phenotype annotations related to respiratory system
Darker colors indicate more annotations
Human Phenotypes
Recurrent aspiration pneumonia
Recurrent respiratory infections
Respiratory insufficiency due to muscle weakness
Respiratory insufficiency
Respiratory failure
Disease(s) Associated with ASAH1
Farber lipogranulomatosis
spinal muscular atrophy with progressive myoclonic epilepsy

Mouse Phenotypes
pulmonary alveolar edema
lung inflammation
abnormal pulmonary alveolus morphology
Availability Mouse Genotype
Asah1tm1.2Geno/Asah1tm1.2Geno
Asah1tm1Medin/Asah1tm1Medin

Contributing Projects:
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
05/14/2024
MGI 6.23
The Jackson Laboratory