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Symbol
Name
ID

Rarb
retinoic acid receptor, beta
MGI:97857

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Micrognathia	Retrognathia	Cleft palate	Broad nasal tip	Wide nasal bridge
Disease(s) Associated with RARB
syndromic microphthalmia 12

Mouse Phenotypes		abnormal basioccipital bone morphology	absent metoptic pillar	fusion of atlas and occipital bones
Availability	Mouse Genotype	abnormal basioccipital bone morphology	absent metoptic pillar	fusion of atlas and occipital bones
	Rarb^tm1Mma/Rarb^tm1Mma
	Rarb^tm1Mma/Rarb⁺

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 04/16/2024 MGI 6.23