Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
congenital stationary night blindness autosomal dominant 2 | DOID:0110863 |
OMIM:163500 |
J:75964 |
Allele Symbol Allele Name Allele ID |
Pde6brd1-3H retinal degeneration 1, 3 Harwell MGI:2178319 |
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Summary |
2 genotypes
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|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
congenital stationary night blindness autosomal dominant 2 | DOID:0110863 |
OMIM:163500 |
J:75964 |
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
congenital stationary night blindness autosomal dominant 2 | DOID:0110863 |
OMIM:163500 |
J:75964 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2018 MGI 6.11 |
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