Symbol
Name
ID
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Synonyms
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3322402L07Rik, rd-3, rd3
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Genetic Map
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(26)
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Alleles
and
phenotypes
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All alleles(2) :
Gene trapped(1)
Spontaneous(1)
| Homozygotes for a spontaneous mutation exhibit retinal degeneration, beginning at 3 weeks of age, characterized by complete loss of photoreceptor rod cells by 5 weeks, and cones by 8 weeks. |
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Polymorphisms
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SNPs within 2kb(75 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (1 records)
Data Summary:
Assays (1)
Results (6)
Tissues (3)
Images (7)
Theiler Stages: 28
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Assay Type |
Assays |
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Results |
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RNA in situ |
1 |
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6 |
cDNA source data(18)
External Resources:
Allen Brain Atlas
GEO
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Molecular
reagents
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All nucleic(19)
cDNA(19)
Microarray probesets(3)
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Other database
links
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References
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(Earliest)
J:4364
Bell JR et al.,
"Genomic structure, chromosomal location, and evolution of the mouse Hox 8 gene [published erratum appears in Genomics 1993 Sep;17(3):800]"
Genomics 1993 Apr;16(1):123-31
(Latest)
J:136923
Danciger M et al.,
"Genetic modifiers of retinal degeneration in the rd3 mouse."
Invest Ophthalmol Vis Sci 2008 Jul;49(7):2863-9
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All references(15)
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Other
accession IDs
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MGD-MRK-13810, MGD-MRK-13813, MGI:97884
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