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Symbol
Name
ID
Fam20a
family with sequence similarity 20, member A
MGI:2388266
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hypophosphaturia
Hypocalciuria
Enuresis
Nephrocalcinosis
Polyuria
Impaired renal concentrating ability
Nephropathy
Renal insufficiency
Disease(s) Associated with FAM20A
amelogenesis imperfecta type 1G

Mouse Phenotypes
abnormal kidney arterial blood vessel morphology
abnormal kidney morphology
dilated renal tubules
Availability Mouse Genotype
Fam20atm1b(KOMP)Wtsi/Fam20atm1b(KOMP)Wtsi
Fam20atm1Lex/Fam20atm1Lex

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