The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RPGRIP1L-20-RE | 20 (40 μL) | 200 μL |  |
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| RPGRIP1L-20-OR | 20 (40 μL) | 200 μL |  |
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| RPGRIP1L-20-GO | 20 (40 μL) | 200 μL |  |
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| RPGRIP1L-20-GR | 20 (40 μL) | 200 μL |  |
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| RPGRIP1L-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]
Gene Symbol : RPGRIP1L
Gene Name : RPGRIP1 like
Chromosome : CHR 16: 537,039,33-535,992,38
Locus : 16q12.2
Alt. Genes : ZNF263
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