Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
laboratory mouse strain
|
| gptkbp:firstDescribed |
2008
|
| gptkbp:hasModel |
human retinal diseases
|
| gptkbp:hasPhenotype |
photoreceptor degeneration
retinal dysplasia |
| https://www.w3.org/2000/01/rdf-schema#label |
rd8 mouse
|
| gptkbp:mutationAssociatedWith |
Crb1 gene
single base deletion in exon 9 of Crb1 |
| gptkbp:origin |
spontaneous mutation in C57BL/6N mice
|
| gptkbp:usedBy |
vision science researchers
|
| gptkbp:usedIn |
retinal degeneration research
|
| gptkbp:bfsParent |
gptkb:CRB1_gene
|
| gptkbp:bfsLayer |
7
|