Symbol Name ID |
Pbx1
pre B cell leukemia homeobox 1 MGI:97495 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal heart morphology |
Vascular dilatation |
Disease(s) Associated with PBX1 | ||
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay |
Mouse Phenotypes | abnormal vasculogenesis |
persistent truncus arteriosus |
ventricular septal defect |
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Availability | Mouse Genotype | |||
Pbx1em1Dunw/Pbx1em1Dunw | ||||
Pbx1tm1.1Febe/Pbx1tm1.1Febe |
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 07/05/2024 MGI 6.24 |
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