Symbol Name ID |
Reln
reelin MGI:103022 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal retinal morphology |
Hypertelorism |
Disease(s) Associated with RELN | ||
Norman-Roberts syndrome |
Mouse Phenotypes | abnormal retina rod bipolar cell morphology |
abnormal retina inner nuclear layer morphology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | ||||
Relnrl-2J/Relnrl-2J |
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 04/16/2024 MGI 6.23 |
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