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Symbol
Name
ID

Pbx1
pre B cell leukemia homeobox 1
MGI:97495

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Congenital diaphragmatic hernia	Generalized hypotonia
Disease(s) Associated with PBX1	Congenital diaphragmatic hernia	Generalized hypotonia
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay

Mouse Phenotypes		diaphragmatic hernia
Availability	Mouse Genotype	diaphragmatic hernia
	Pbx1^tm1Mlc/Pbx1^tm1Mlc

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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