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Symbol
Name
ID

Acvr2b
activin receptor IIB
MGI:87912

Phenotype annotations related to skeleton

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Congenital hip dislocation	Block vertebrae	Short long bone	Absence of the sacrum
Disease(s) Associated with ACVR2B
visceral heterotaxy

Mouse Phenotypes		abnormal rib morphology	rib fusion	increased thoracic vertebrae number	thoracic vertebral transformation	lumbar vertebral transformation	sacral vertebral transformation	vertebral transformation
Availability	Mouse Genotype	abnormal rib morphology	rib fusion	increased thoracic vertebrae number	thoracic vertebral transformation	lumbar vertebral transformation	sacral vertebral transformation	vertebral transformation
	Acvr2b^tm1.1Spo/Acvr2b^tm1.1Spo
	Acvr2b^tm1Enl/Acvr2b^tm1Enl
	Acvr2b^tm1Spo/Acvr2b^tm1Spo							!

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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