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Symbol
Name
ID

Foxp1
forkhead box P1
MGI:1914004

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Flexion contracture	Spasticity	Hypotonia	Generalized hypotonia
Disease(s) Associated with FOXP1
intellectual disability-severe speech delay-mild dysmorphism syndrome

Mouse Phenotypes		thin ventricle myocardium compact layer	disorganized myocardium	abnormal fetal cardiomyocyte proliferation	increased fetal cardiomyocyte proliferation	abnormal sarcomere morphology
Availability	Mouse Genotype	thin ventricle myocardium compact layer	disorganized myocardium	abnormal fetal cardiomyocyte proliferation	increased fetal cardiomyocyte proliferation	abnormal sarcomere morphology
	Foxp1^tm1Eem/Foxp1^tm1Eem
	Foxp1^tm2.1Eem/Foxp1^tm2.1Eem Nkx2-5^tm1(cre)Rjs/Nkx2-5⁺ (conditional)
	Foxp1^tm2.1Eem/Foxp1^tm2.1Eem Tg(Tek-cre)1Ywa/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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