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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Rxrb
retinoid X receptor beta
MGI:98215
43 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Nr1h2tm1.1Gstr/Nr1h2+
Rxrbtm1Mma/Rxrb+
involves: 129 * C57BL/6 		abnormal Sertoli cell morphology J:101966
Rarbtm1Vgi/Rarbtm1Vgi
Rxrbtm1Rev/Rxrbtm1Rev
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 		abnormal excitatory postsynaptic potential J:51892
abnormal spatial learning J:51892
absent long-term depression J:51892
reduced long-term potentiation J:51892
Rxratm1.1Pcn/Rxratm1.1Pcn
Rxrbtm1Ipc/Rxrbtm1Ipc
involves: 129S2/SvPas * C57BL/6 * SJL 		normal embryo phenotype J:146761
embryonic growth retardation J:146761
Rxratm1Ipc/Rxratm1Ipc
Rxrbtm1Mma/Rxrbtm1Mma
involves: 129S2/SvPas * C57BL/6 		abnormal conotruncus septation J:146761
abnormal cornea stroma morphology J:146761
abnormal eye development J:146761
abnormal eyelid morphology J:146761
abnormal ocular fundus morphology J:146761
abnormal retina morphology J:146761
optic disk coloboma J:146761
ventral rotation of lens J:146761
ventricular myocardium compact layer hypoplasia J:146761
Rxratm1Ipc/Rxratm4Ipc
Rxrbtm1Mma/Rxrbtm1Pcn
Tg(KRT14-cre)1Ipc/0
involves: 129S2/SvPas * C57BL/6 * SJL 		abnormal epidermis stratum corneum morphology J:109090
abnormal keratinocyte morphology J:109090
abnormal skin condition J:109090
abnormal skin morphology J:109090
Rxratm1Ipc/Rxratm4Ipc
Rxrbtm1Mma/Rxrbtm1Pcn
Tg(KRT14-cre/ERT2)1Ipc/0
involves: 129S2/SvPas 		abnormal epidermis stratum corneum morphology J:109090
abnormal keratinocyte morphology J:109090
abnormal skin morphology J:109090
alopecia J:102470
dermal hyperplasia J:102470
epidermal hyperplasia J:102470
hair follicle degeneration J:102470
increased immunoglobulin level J:102470
mixed cellular infiltration to dermis J:102470
Rxratm2Ipc/Rxratm2Ipc
Rxrbtm1Mma/Rxrbtm1Mma
involves: 129/Sv * C57BL/6 		abnormal otic vesicle development J:146761
absent third pharyngeal arch artery J:146761
normal embryo phenotype J:146761
increased rhombomere 5 size J:146761
third pharyngeal arch hypoplasia J:146761
Rxratm4Ipc/Rxratm4Ipc
Rxrbtm1Pcn/Rxrbtm1Pcn
Tg(KRT14-cre)1Ipc/0
involves: 129S2/SvPas * C57BL/6 * SJL 		abnormal epidermis stratum corneum morphology J:109090
abnormal keratinocyte morphology J:109090
decreased cholesterol level J:109090
shiny skin J:109090
Rxratm4Ipc/Rxratm4Ipc
Rxrbtm1Pcn/Rxrbtm1Pcn
Tg(KRT14-cre/ERT2)1Ipc/0
involves: 129S2/SvPas 		alopecia J:102470
dermal cyst J:102470
dermatitis J:102470
dry skin J:102470
ear inflammation J:102470
enlarged cervical lymph nodes J:102470
enlarged liver J:102470
enlarged spleen J:102470
epidermal hyperplasia J:102470
hair follicle degeneration J:102470
increased leukocyte cell number J:102470
lymph node hyperplasia J:102470
mixed cellular infiltration to dermis J:102470
scaly skin J:102470
skin lesions J:102470
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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory