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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxl1
forkhead box L1
MGI:1347469
22 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Foxl1tm1Hfk/Foxl1tm1Hfk
C.129-Foxl1tm1Hfk
abnormal crypts of Lieberkuhn morphology J:111077
ectopic Paneth cells J:111077
Foxl1tm1Hfk/Foxl1tm1Hfk
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal digestive secretion J:76379
abnormal gastric chief cell morphology J:76379
abnormal gastric gland morphology J:76379
abnormal gastric parietal cell morphology J:76379
abnormal pyloric gastric gland morphology J:76379
decreased body size J:76379
increased stomach mucosa thickness J:76379
Foxl1tm1Khk/Foxl1tm1Khk
involves: 129P2/OlaHsd * C57BL/6
abnormal intestinal epithelium morphology J:41235
abnormal intestinal goblet cell morphology J:41235
abnormal jejunum morphology J:41235
abnormal small intestinal villus morphology J:41235
abnormal small intestine crypts of Lieberkuhn morphology J:41235
abnormal stomach glandular epithelium morphology J:41235
abnormal stomach morphology J:41235
abnormal stomach mucosa morphology J:41235
decreased small intestinal villus size J:41235
delayed intestine development J:41235
normal neoplasm J:95893
postnatal growth retardation J:41235
postnatal lethality, incomplete penetrance J:41235

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
04/30/2024
MGI 6.23
The Jackson Laboratory