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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fgd4
FYVE, RhoGEF and PH domain containing 4
MGI:2183747
10 phenotypes from 3 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fgd4tm1.1Ics/Fgd4tm1.1Ics
Not Specified
abnormal action potential J:190437
abnormal myelin sheath morphology J:190437
abnormal myelination J:190437
abnormal nervous system electrophysiology J:190437
decreased grip strength J:190437
decreased nerve conduction velocity J:190437
demyelination J:190437
Fgd4tm1a(EUCOMM)Wtsi/Fgd4tm1a(EUCOMM)Wtsi
C57BL/6N-Fgd4tm1a(EUCOMM)Wtsi/Wtsi
decreased lean body mass J:211773
increased lean body mass J:211773
Fgd4tm1Ics/Fgd4tm1Ics
Mnx1tm4(cre)Tmj/Mnx1+
involves: 129S1/Sv
normal nervous system phenotype J:190437
Fgd4tm1Ics/Fgd4tm1Ics
Tg(Dhh-cre)1Mejr/0
involves: FVB/N
abnormal myelination J:190437
Fgd4tm1Ics/Fgd4tm1Ics
Tg(Plp1-cre/ERT2)1Ueli/0
involves: C57BL/6 * DBA/2
abnormal myelin sheath morphology J:190437

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
09/10/2019
MGI 6.14
The Jackson Laboratory