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Symbol
Name
ID
Rbpj
recombination signal binding protein for immunoglobulin kappa J region
MGI:96522
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Oligohydramnios
Decreased fetal movement
Disease(s) Associated with RBPJ
Adams-Oliver syndrome

Mouse Phenotypes
abnormal placental labyrinth vasculature morphology
absent vitelline blood vessels
embryonic growth retardation
abnormal neural tube morphology
abnormal melanoblast morphology
decreased spongiotrophoblast size
abnormal decidualization
abnormal vitelline vascular remodeling
Availability Mouse Genotype
Rbpjtm1Kyo/Rbpjtm1Kyo
Pax3tm1(cre)Joe/Pax3+
Rbpjtm1Hon/Rbpjtm1Hon  (conditional)
Rbpjtm1Hon/Rbpjtm1Hon
Tg(Tyr-cre)#Lru/0  (conditional)
Pgrtm2(cre)Lyd/Pgr+
Rbpjtm1Hon/Rbpjtm1Hon  (conditional)
Rbpjtm1Hon/Rbpjtm1.1Hon
Tg(Pax7-cre/ERT2)1Cbm/0  (conditional)
Rbpjtm1Kyo/Rbpjtm1Hon
Tg(Tek-cre)12Flv/0  (conditional)

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory