Symbol Name ID |
Asah1
N-acylsphingosine amidohydrolase 1 MGI:1277124 |
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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/14/2024 MGI 6.23 |
|
|