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Symbol
Name
ID
Ift172
intraflagellar transport 172
MGI:2682064
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Proteinuria
Nephronophthisis
Chronic kidney disease
Disease(s) Associated with IFT172
Bardet-Biedl syndrome 20
short-rib thoracic dysplasia 10 with or without polydactyly

Mouse Phenotypes
abnormal kidney morphology
abnormal renal glomerulus morphology
Availability Mouse Genotype
Ift172avc1/Ift172avc1

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
04/23/2024
MGI 6.23
The Jackson Laboratory