|
Symbol Name ID |
Spart
spartin MGI:2139806 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Genu valgum |
Abnormal thumb morphology |
Hammertoe |
Clinodactyly |
Brachydactyly |
Short foot |
Ankle clonus |
Flexion contracture |
Camptodactyly |
Joint hypermobility |
Hyperextensible hand joints |
Abnormality of the skeletal system |
Kyphoscoliosis |
| Disease(s) Associated with SPART | ||||||||||||||
| Troyer syndrome |
| Mouse Phenotypes | skeleton phenotype |
abnormal chondrocyte morphology |
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| Availability | Mouse Genotype | ||
| Sparttm1.1Xen/Sparttm1.1Xen | * | ||
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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