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Symbol Name ID |
Sms
spermine synthase MGI:109490 |
| Darker colors indicate more annotations |
| Human Phenotypes | Camptodactyly |
Hypotonia |
Generalized hypotonia |
Infantile muscular hypotonia |
Difficulty standing |
Decreased muscle mass |
| Disease(s) Associated with SMS | ||||||
| syndromic X-linked intellectual disability Snyder type |
| Mouse Phenotypes | muscle weakness |
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| Availability | Mouse Genotype | |
| Smstm1a(EUCOMM)Wtsi/Y | ||
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 04/09/2024 MGI 6.23 |
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