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Symbol Name ID |
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| Feature Type | protein coding gene | ||||||||||||||||||
| Genetic Map | |||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:12866 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken Protein SuperFamily: complement subcomponent C1q chain A Gene Tree: Mfrp |
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| Human homologs |
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Alleles and phenotypes |
All alleles(2) :
Spontaneous(2)
Mutations produce mice having small, white retinal spots and progressive photoreceptor degeneration. Human Diseases Modeled Using Mouse Mfrp (1) Alleles Annotated to Human Diseases(1) |
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Gene Ontology (GO) classifications |
All GO classifications: (3 annotations)
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| Expression |
cDNA source data(1) External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(3)
cDNA(1)
Other(2)
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Other database links |
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| Sequences |
All sequences(23) RefSeq(4) |
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| Polymorphisms | SNPs(38 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:64087
Hawes NL, et al., Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens. Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57 (Latest) J:181596 Fogerty J, et al., 174delG mutation in mouse MFRP causes photoreceptor degeneration and RPE atrophy. Invest Ophthalmol Vis Sci. 2011 Sep;52(10):7256-66 All references(19) |
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Other accession IDs |
MGI:1888693 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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