The protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
CNGA1BA-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
CNGA1BA-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Symbol : CNGA1
Gene Name : Cyclic nucleotide gated channel alpha 1
Chromosome : CHR 4: 480,167,17-479,350,14
Locus : 4p12
Alt. Genes : FAM13A
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