Symbol Name ID |
Hsd17b4
hydroxysteroid (17-beta) dehydrogenase 4 MGI:105089 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertelorism |
Undetectable electroretinogram |
Strabismus |
Nystagmus |
Limited extraocular movements |
Visual loss |
Disease(s) Associated with HSD17B4 | ||||||
D-bifunctional protein deficiency | ||||||
Perrault syndrome |
Mouse Phenotypes | abnormal eye morphology |
abnormal iris morphology |
irregularly shaped pupil |
cataract |
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Availability | Mouse Genotype | ||||
Hsd17b4em1(IMPC)Tcp/Hsd17b4em1(IMPC)Tcp | |||||
Hsd17b4tm1Baes/Hsd17b4tm1Baes |
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 09/03/2024 MGI 6.24 |
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