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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
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
Foxp1tm1Eem/Foxp1tm1Eem
Foxp1tm2.1Eem/Foxp1tm2.1Eem
Nkx2-5tm1(cre)Rjs/Nkx2-5+  (conditional)
Foxp1tm2.1Eem/Foxp1tm2.1Eem
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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last database update
01/07/2020
MGI 6.14
The Jackson Laboratory