Symbol Name ID |
Adamts3
ADAM metallopeptidase with thrombospondin type 1 motif 3 MGI:3045353 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Craniosynostosis |
Coronal craniosynostosis |
Retrognathia |
Malar flattening |
Camptodactyly of finger |
Syndactyly |
Cutaneous finger syndactyly |
Finger syndactyly |
Short foot |
Short palm |
Small hand |
Joint contracture of the hand |
Camptodactyly |
Delayed skeletal maturation |
Hypoplastic iliac wing |
Pectus excavatum |
Narrow chest |
Scoliosis |
Osteoporosis |
Disease(s) Associated with ADAMTS3 | |||||||||||||||||||
Hennekam syndrome |
Mouse Phenotypes | skeleton phenotype |
basisphenoid bone foramen |
abnormal cervical rib |
fusion of vertebral arches |
|
Availability | Mouse Genotype | ||||
Adamts3tm1.2Itl/Adamts3tm1.2Itl | * | ||||
Adamts3tm1b(KOMP)Wtsi/Adamts3tm1b(KOMP)Wtsi |
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 04/23/2024 MGI 6.23 |
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