Symbol
Name
ID

Adamts3
ADAM metallopeptidase with thrombospondin type 1 motif 3
MGI:3045353

Phenotype annotations related to skeleton

*	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	skeleton phenotype	basisphenoid bone foramen	abnormal cervical rib	fusion of vertebral arches
	Adamts3^tm1.2Itl/Adamts3^tm1.2Itl	*
	Adamts3^{tm1b(KOMP)Wtsi}/Adamts3^{tm1b(KOMP)Wtsi}

Contributing Projects: 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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