CNGA1 Break Apart FISH Probe

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 Details
SKU Test Kits Buffer Dye Color Order Now
CNGA1BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
CNGA1BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

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 Details

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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