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Symbol Name ID |
Spred2
sprouty-related EVH1 domain containing 2 MGI:2150019 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Clinodactyly of the 5th finger |
Brachydactyly |
Radioulnar synostosis |
Joint hypermobility |
Delayed skeletal maturation |
Enlarged thorax |
Pectus carinatum |
Pectus excavatum |
Scoliosis |
Osteopenia |
| Disease(s) Associated with SPRED2 | |||||||||||
| Noonan syndrome |
| Mouse Phenotypes | short tibia |
decreased width of hypertrophic chondrocyte zone |
decreased long bone epiphyseal plate size |
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| Availability | Mouse Genotype | |||
| Spred2Gt(XB228)Byg/Spred2Gt(XB228)Byg | ||||
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 04/30/2024 MGI 6.23 |
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