Symbol Name ID |
Nyx
nyctalopin MGI:2448607 |
Darker colors indicate more annotations |
Human Phenotypes | Congenital stationary night blindness |
High myopia |
Hemeralopia |
Disease(s) Associated with NYX | |||
congenital stationary night blindness 1A |
Mouse Phenotypes | abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
absent visual evoked potential |
abnormal vision |
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Availability | Mouse Genotype | |||||
Nyxnob/Nyxnob | ||||||
Nyxnob/Nyx+ | ||||||
Nyxnob/Y |
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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