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Symbol
Name
ID

Rnf220
ring finger protein 220
MGI:1913993

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Spastic paraplegia	CNS hypomyelination	Peripheral axonal neuropathy	Thin corpus callosum	Ataxia	Dysarthria	Intellectual disability	Hyperreflexia	Motor delay	Seizure
Disease(s) Associated with RNF220
hypomyelinating leukodystrophy 23

Mouse Phenotypes		abnormal neural tube morphology	decreased motor neuron number	abnormal ventral interneuron morphology	abnormal ventral interneuron 0 morphology	abnormal ventral interneuron 1 morphology	abnormal ventral interneuron 2 morphology	abnormal ventral interneuron 3 morphology
Availability	Mouse Genotype	abnormal neural tube morphology	decreased motor neuron number	abnormal ventral interneuron morphology	abnormal ventral interneuron 0 morphology	abnormal ventral interneuron 1 morphology	abnormal ventral interneuron 2 morphology	abnormal ventral interneuron 3 morphology
	Rnf220^em1Chek/Rnf220^em1Chek
	Tg(Ddx4-cre)1Dcas/0 Rnf220^em1Kust/Rnf220^em1Kust (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/14/2024 MGI 6.23