Rxra Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rxra
retinoid X receptor alpha
MGI:98214

39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Rarg^tm2Ipc/Rarg^tm2Ipc Rxra^tm2Ipc/Rxra^tm2Ipc involves: 129/Sv * 129S2/SvPas	abnormal anterior eye segment morphology	J:42773
Rarg^tm4Ipc/Rarg^tm4Ipc Rxra^tm2Ipc/Rxra^tm2Ipc involves: 129	abnormal anterior eye segment morphology	J:42773
Rxra^tm1.1Pcn/Rxra^tm1.1Pcn Rxrb^tm1Ipc/Rxrb^tm1Ipc involves: 129S2/SvPas * C57BL/6 * SJL	normal embryo phenotype	J:146761
	embryonic growth retardation	J:146761
Rxra^tm1Ipc/Rxra^tm1Ipc Rxrb^tm1Mma/Rxrb^tm1Mma 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
Rxra^tm1Ipc/Rxra^tm4Ipc Rxrb^tm1Mma/Rxrb^tm1Pcn 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
Rxra^tm1Ipc/Rxra^tm4Ipc Rxrb^tm1Mma/Rxrb^tm1Pcn 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
Rxra^tm2Ipc/Rxra^tm2Ipc Rxrb^tm1Mma/Rxrb^tm1Mma 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
Rxra^tm4Ipc/Rxra^tm4Ipc Rxrb^tm1Pcn/Rxrb^tm1Pcn 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
Rxra^tm4Ipc/Rxra^tm4Ipc Rxrb^tm1Pcn/Rxrb^tm1Pcn 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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