Symbol Name ID |
Smpd1
sphingomyelin phosphodiesterase 1, acid lysosomal MGI:98325 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Arthralgia |
Disease(s) Associated with SMPD1 | ||
Niemann-Pick disease type A | ||
Niemann-Pick disease type B |
Mouse Phenotypes | lethargy |
abnormal depression-related behavior |
tremors |
ataxia |
impaired coordination |
hunched posture |
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Availability | Mouse Genotype | ||||||
Smpd1tm1Esc/Smpd1tm1Esc | |||||||
Smpd1tm1Wst/Smpd1tm1Wst |
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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