|
Symbol Name ID |
Sms
spermine synthase MGI:109490 |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
Thickened calvaria |
Mandibular prognathia |
Short neck |
Hyperextensibility of the finger joints |
Long fingers |
Arachnodactyly |
Long hallux |
Long toe |
Slender toe |
Camptodactyly |
Recurrent fractures |
Pectus carinatum |
Pectus excavatum |
Kyphosis |
Kyphoscoliosis |
Scoliosis |
Vertebral compression fracture |
Osteoporosis |
Thin bony cortex |
| Disease(s) Associated with SMS | ||||||||||||||||||||
| syndromic X-linked intellectual disability Snyder type |
| Mouse Phenotypes | abnormal spine curvature |
lordosis |
decreased bone mineral content |
decreased bone mineral density |
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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 04/16/2024 MGI 6.23 |
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