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18 records found for search term C1qtnf5
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1308802C1qtnf5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membrane85334775453349912Rat86symbol , PhenoGengene, protein-coding, PROVISIONAL [RefSeq]
1318784C1QTNF5C1q and TNF related 5This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequenc11119338942119346705Human127symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1553055C1qtnf5C1q and tumor necrosis factor related protein 5The protein encoded by this gene is a member of the C1q/tumor necrosis factor superfamily. This family member is a secretory protein that functions in eye development. Mutations in this gene are thought to underlie the pathophysiology of late-onset retinal degeneration (L-ORD) and early-onset long a94401306744020484Mouse119symbol , PhenoGen , descriptiongene, protein-coding, REVIEWED [RefSeq]
8995558C1qtnf5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membraneNW_0049554122041975420421541Chinchilla24symbolgene, protein-coding, MODEL [RefSeq]
11880623C1QTNF5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (inferred); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membrane11114179998114187761Bonobo22symbolgene, protein-coding, MODEL [RefSeq]
12270802C1QTNF5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (inferred); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membrane51456111514563277Dog26symbolgene, protein-coding, MODEL [RefSeq]
12567008C1qtnf5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (inferred); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membraneNW_00493654242696364271497Squirrel26symbolgene, protein-coding, MODEL [RefSeq]
155247035c1qtnf5Tropical Clawed Frogsymbolgene, null
625922835C1qtnf5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membraneBlack Rat24symbolgene, protein-coding, MODEL [RefSeq]
18383568C1QTNF5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (inferred); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membraneGreen Monkey26symbolgene, protein-coding, MODEL [RefSeq]
14154533C1QTNF5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (inferred); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membranePig26symbolgene, protein-coding, MODEL [RefSeq]
18914719C1qtnf5C1q and TNF related 5ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN inner ear development (ortholog); protein secretion (ortholog); ASSOCIATED WITH isolated microphthalmia 5 (ortholog); late-onset retinal degeneration (ortholog); lens disease (ortholog); FOUND IN apical plasma membraneNaked Mole-Rat24symbolgene, protein-coding, MODEL [RefSeq]
626468171c1qtnf5.LAfrican Clawed Frogsymbolgene, null
626174290c1qtnf5.SAfrican Clawed Frogsymbolgene, null
626181927c1qtnf5.SAfrican Clawed Frogsymbolgene, null
626171576c1qtnf5.SAfrican Clawed Frogsymbolgene, null
1620492Mfrpmembrane frizzled-related proteinThe protein encoded by this gene contains a region with similarity to the cysteine-rich domain (CRD) of frizzled, a gene originally found in Drosophila that controls tissue polarity. This protein functions in eye development, where it is necessary for the maintenance of photoreceptor outer segments.94401306744020484Mouse67descriptiongene, protein-coding, REVIEWED [RefSeq]
1316695MFRPmembrane frizzled-related proteinThis gene encodes a member of the frizzled-related protein family. The encoded protein plays an important role in eye development and mutations in this gene have been associated with nanophthalmos, posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc drusen. The protein is en11119338942119346705Human88descriptiongene, protein-coding, REVIEWED [RefSeq]