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Symbol
Name
ID

Rnf2
ring finger protein 2
MGI:1101759

Phenotype annotations related to skeleton

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Primary microcephaly	Short foot	Small hand
Disease(s) Associated with RNF2
Luo-Schoch-Yamamoto syndrome

Mouse Phenotypes		skeleton phenotype	abnormal sternum ossification	thoracic vertebral transformation	cervical vertebral transformation
Availability	Mouse Genotype	skeleton phenotype	abnormal sternum ossification	thoracic vertebral transformation	cervical vertebral transformation
	Rnf2^tm1Hko/Rnf2^tm1Hko
	Rnf2^tm3Hko/Rnf2^tm3Hko	*

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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