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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxc1
forkhead box C1
MGI:1347466
64 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Foxc1tm1Blh/Foxc1+
Tyrc-2J/Tyrc-2J
B6.Cg-Tyrc-2J Foxc1tm1Blh
abnormal aqueous drainage system morphology J:82280
abnormal trabecular meshwork morphology J:82280
absent Schlemm's canal J:82280
iris synechia J:82280
Foxc1tm1Blh/Foxc1+
Foxc2tm1Blh/Foxc2+
involves: 129S6/SvEvTac * Black Swiss
abnormal aortic valve morphology J:57677
abnormal branching involved in ureteric bud morphogenesis J:60834
abnormal canal of Schlemm morphology J:61775
abnormal ciliary body morphology J:61775
abnormal cornea morphology J:61775
abnormal fourth pharyngeal arch artery morphology J:57677
abnormal iridocorneal angle J:61775
abnormal iris morphology J:61775
abnormal mesonephros morphology J:60834
abnormal pharyngeal arch artery morphology J:57677
abnormal pulmonary valve morphology J:57677
abnormal superior vena cava morphology J:57677
abnormal trabecular meshwork morphology J:61775
absent kidney J:60834
aortic arch coarctation J:57677
cornea ulcer J:61775
cornea vascularization J:61775
decreased angiogenesis J:57677
double ureter J:60834
duplex kidney J:60834
ectopic ureteric bud J:60834
enlarged liver J:57677
eyelids open at birth J:61775
hydronephrosis J:60834
hydrops fetalis J:57677
hydroureter J:60834
interrupted aortic arch, type b J:57677
iris stroma hypoplasia J:61775
lethality throughout fetal growth and development, incomplete penetrance J:57677
perimembraneous ventricular septal defect J:57677
renal hypoplasia J:60834
normal skeleton phenotype J:57677
thick aortic valve cusps J:57677
thick pulmonary valve cusps J:57677
trabecula carnea hypoplasia J:57677
ventricle myocardium hypoplasia J:57677
Foxc1tm1Blh/Foxc1+
Foxc2tm1Blh/Foxc2tm1Blh
involves: 129S6/SvEvTac
abnormal mesonephros morphology J:91443
abnormal somite shape J:91443
Foxc1tm1Blh/Foxc1+
Foxc2tm1Blh/Foxc2tm1Blh
involves: 129S6/SvEvTac * Black Swiss
abnormal pharyngeal arch artery morphology J:71693
abnormal somite shape J:71693
abnormal vascular development J:71693
absent second pharyngeal arch J:71693
decreased somite size J:71693
embryonic lethality during organogenesis, complete penetrance J:71693
enlarged third pharyngeal arch artery J:71693
Foxc1tm1Blh/Foxc1tm1Blh
Foxc2tm1Blh/Foxc2+
involves: 129S6/SvEvTac
normal embryo phenotype J:91443
Foxc1tm1Blh/Foxc1tm1Blh
Foxc2tm1Blh/Foxc2+
involves: 129S6/SvEvTac * Black Swiss
normal cardiovascular system phenotype J:71693
embryonic lethality during organogenesis, complete penetrance J:71693
Foxc1tm1Blh/Foxc1tm1Blh
Foxc2tm1Blh/Foxc2tm1Blh
involves: 129S6/SvEvTac
abnormal mesonephros morphology J:91443
abnormal somite development J:91443
absent somites J:91443
normal embryo phenotype J:91443
Foxc1tm1Blh/Foxc1tm1Blh
Foxc2tm1Blh/Foxc2tm1Blh
involves: 129S6/SvEvTac * Black Swiss
abnormal dorsal aorta morphology J:71693
abnormal dorsal-ventral polarity of the somites J:71693
abnormal head development J:71693
abnormal heartbeat J:71693
abnormal pharyngeal pouch morphology J:71693
abnormal vascular development J:71693
abnormal vitelline vascular remodeling J:71693
absent paraxial mesoderm J:71693
absent second pharyngeal arch J:71693
absent somites J:71693
decreased embryo size J:71693
dilated dorsal aorta J:71693
disorganized myocardium J:71693
embryonic lethality during organogenesis, complete penetrance J:71693
enlarged pericardium J:71693
head mesenchyme hypoplasia J:71693
incomplete rostral neuropore closure J:71693
small first pharyngeal arch J:71693
small heart J:71693

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
12/10/2024
MGI 6.24
The Jackson Laboratory