The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CUL7-20-RE | 20 (40 μL) | 200 μL |  |
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| CUL7-20-OR | 20 (40 μL) | 200 μL |  |
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| CUL7-20-GO | 20 (40 μL) | 200 μL |  |
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| CUL7-20-GR | 20 (40 μL) | 200 μL |  |
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| CUL7-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
Gene Symbol : CUL7
Gene Name : Cullin 7
Chromosome : CHR 6: 430,539,49-430,376,16
Locus : 6p21.1
Alt. Genes : AASS
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