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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fam20a
family with sequence similarity 20, member A
MGI:2388266
22 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fam20atm1b(KOMP)Wtsi/Fam20atm1b(KOMP)Wtsi
C57BL/6N-Fam20atm1b(KOMP)Wtsi/Ucd
abnormal kidney morphology J:211773
short tibia J:211773
Fam20atm1Lex/Fam20a+
involves: 129S5/SvEvBrd * C57BL/6
postnatal lethality, incomplete penetrance J:186384
Fam20atm1Lex/Fam20atm1Lex
involves: 129S5/SvEvBrd * C57BL/6
abnormal ameloblast morphology J:186384
abnormal enamel morphology J:186384
abnormal enamel rod pattern J:186384
abnormal incisor morphology J:186384
abnormal kidney arterial blood vessel morphology J:186384
abnormal kidney morphology J:186384
abnormal lower incisor color J:186384
abnormal molar cusp morphology J:186384
abnormal molar morphology J:186384
abnormal tooth wear J:186384
abnormal upper incisor color J:186384
absent enamel J:186384
calcified artery J:186384
calcified pulmonary alveolus J:186384
conical molar J:186384
dilated renal tubules J:186384
enamel pits J:186384
normal growth/size/body region phenotype J:186384
normal mortality/aging J:186384
small molars J:186384

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
03/24/2020
MGI 6.15
The Jackson Laboratory