Rarb Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rarb
retinoic acid receptor, beta
MGI:97857

38 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rarb^{em1(IMPC)Kmpc}/Rarb^{em1(IMPC)Kmpc} C57BL/6NTac-Rarb^{em1(IMPC)Kmpc}/Kmpc	abnormal cornea morphology	J:211773
	abnormal lens morphology	J:211773
	cataract	J:211773
	cornea opacity	J:211773
	decreased total body fat amount	J:211773
	narrow eye opening	J:211773
Rarb^tm1Ipc/Rarb^tm1Ipc involves: 129S2/SvPas	no abnormal phenotype detected	J:21486
Rarb^tm1Ipc/Rarb^tm1Ipc involves: 129S2/SvPas * C57BL/6	persistent hyperplastic primary vitreous	J:43344
Rarb^tm1Mma/Rarb⁺ involves: 129S2/SvPas * C57BL/6	absent metoptic pillar	J:43344
Rarb^tm1Mma/Rarb⁺ involves: 129S2/SvPas * C57BL/6	narrow eye opening	J:43344
Rarb^tm1Mma/Rarb^tm1Mma involves: 129S2/SvPas * C57BL/6	abnormal basioccipital bone morphology	J:43344
	abnormal lung alveolus development	J:124466
	abnormal lung development	J:124466
	abnormal pulmonary alveolar sac morphology	J:124466
	abnormal skeleton morphology	J:43344
	abnormal vertebral arch morphology	J:43344
	absent metoptic pillar	J:43344
	cataract	J:43344
	cervical vertebral transformation	J:43344
	decreased body weight	J:43344
	fusion of atlas and occipital bones	J:43344
	fusion of atlas and odontoid process	J:43344
	fusion of vertebral arches	J:43344
	normal limbs/digits/tail phenotype	J:43344
	narrow eye opening	J:43344
	normal nervous system phenotype	J:43344
	persistence of hyaloid vascular system	J:43344
	persistent hyperplastic primary vitreous	J:43344
	postnatal growth retardation	J:43344
	retina fold	J:43344
	split cervical atlas	J:43344
	split cervical axis	J:43344
	vertebral transformation	J:43344
	vitreous body deposition	J:43344
Rarb^tm1Vgi/Rarb^tm1Vgi involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal excitatory postsynaptic potential	J:51892
	abnormal lung development	J:110539
	abnormal pulmonary alveolar duct morphology	J:110539
	abnormal pulmonary alveolar sac morphology	J:110539
	abnormal pulmonary alveolar system morphology	J:110539
	abnormal respiratory function	J:110539
	abnormal spatial learning	J:51892
	absent long-term depression	J:51892
	decreased body weight	J:110539
	decreased pulmonary endothelial cell surface	J:110539
	impaired lung alveolus development	J:110539
	reduced long-term potentiation	J:51892
Rarb^tm2.1Ipc/Rarb^tm2.1Ipc involves: C57BL/6 * SJL	persistent hyperplastic primary vitreous	J:75134

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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