Symbol Name ID |
Bbs4
Bardet-Biedl syndrome 4 MGI:2143311 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal degeneration |
Rod-cone dystrophy |
Nyctalopia |
Disease(s) Associated with BBS4 | |||
Bardet-Biedl syndrome 4 |
Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal photoreceptor inner segment morphology |
abnormal photoreceptor outer segment morphology |
optic nerve atrophy |
abnormal retina pigment epithelium morphology |
abnormal posterior eye segment morphology |
abnormal ocular fundus morphology |
abnormal retina morphology |
abnormal retina photoreceptor layer morphology |
increased susceptibility to age-related retinal degeneration |
retina degeneration |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
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Availability | Mouse Genotype | |||||||||||||
Bbs4Gt1Nk/Bbs4Gt1Nk | ||||||||||||||
Bbs4tm1Vcs/Bbs4tm1Vcs |
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 07/05/2024 MGI 6.24 |
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