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Symbol Name ID |
Sprtn
SprT-like N-terminal domain MGI:2685351 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Micrognathia |
Clinodactyly |
Elbow flexion contracture |
Delayed skeletal maturation |
Down-sloping shoulders |
Pectus excavatum |
Thoracic kyphoscoliosis |
Osteoporosis |
| Disease(s) Associated with SPRTN | |||||||||
| Ruijs-Aalfs syndrome |
| Mouse Phenotypes | skeleton phenotype |
kyphosis |
lordosis |
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| Availability | Mouse Genotype | |||
| Sprtntm1Yjm/Sprtntm1Yjm | * | |||
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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