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Symbol
Name
ID

Rrm2b
ribonucleotide reductase M2 B (TP53 inducible)
MGI:2155865

Phenotype annotations related to digestive/alimentary system

Darker colors indicate more annotations

Human Phenotypes	Dysphagia
Disease(s) Associated with RRM2B	Dysphagia
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5

Mouse Phenotypes		abnormal submandibular gland morphology
Availability	Mouse Genotype	abnormal submandibular gland morphology
	Rrm2b^tm1Ynak/Rrm2b^tm1Ynak

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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