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Symbol
Name
ID

Pbx1
pre B cell leukemia homeobox 1
MGI:97495

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

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

Mouse Phenotypes		palatal shelf hypoplasia	cleft secondary palate	small snout	abnormal outer ear morphology	outer ear hypoplasia	decreased body size	abnormal embryonic growth/weight/body size
Availability	Mouse Genotype	palatal shelf hypoplasia	cleft secondary palate	small snout	abnormal outer ear morphology	outer ear hypoplasia	decreased body size	abnormal embryonic growth/weight/body size
	Pbx1^em1Dunw/Pbx1^em1Dunw
	Pbx1^tm1.1Febe/Pbx1^tm1.1Febe
	Pbx1^tm1Mlc/Pbx1^tm1Mlc
	Pbx1^tm1Mlc/Pbx1⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23