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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxd1
forkhead box D1
MGI:1347463
23 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Foxd1tm1Lai/Foxd1tm1Lai
either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)
abnormal adrenal gland morphology J:33767
abnormal forebrain morphology J:33767
abnormal kidney development J:33767
abnormal metanephric mesenchyme morphology J:33767
abnormal nephrogenic mesenchyme morphogenesis J:33767
abnormal nephrogenic zone morphology J:33767
abnormal nephron morphology J:33767
abnormal retina morphology J:33767
abnormal ureter morphology J:33767
aphagia J:33767
decreased renal glomerulus number J:33767
delayed kidney development J:33767
dilated kidney collecting duct J:33767
fused kidneys J:33767
impaired branching involved in ureteric bud morphogenesis J:33767
meteorism J:33767
neonatal lethality, complete penetrance J:33767
pelvic kidney J:33767
normal renal/urinary system phenotype J:33767
short ureter J:33767
small adrenal glands J:33767
small kidney J:33767
tachypnea J:33767

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
04/16/2024
MGI 6.23
The Jackson Laboratory