Symbol Name ID |
Ift172
intraflagellar transport 172 MGI:2682064 |
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 |
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Availability | Mouse Genotype | ||
Ift172avc1/Ift172avc1 |
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 |
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