RecName: Full=Cyclic nucleotide-gated channel beta-1; Short=CNG channe - Protein

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Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases. [Genes (Basel). 2021]
Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases.
Mauro-Herrera M, Chiang J, Radojevic B, Bennett LD. Genes (Basel). 2021 Jun 29; 12(7). Epub 2021 Jun 29.
CNGB1-related rod-cone dystrophy: A mutation review and update. [Hum Mutat. 2021]
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, et al. Hum Mutat. 2021 Jun; 42(6):641-666. Epub 2021 May 16.
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. [Ophthalmic Genet. 2021]
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1.
Radojevic B, Jones K, Klein M, Mauro-Herrera M, Kingsley R, Birch DG, Bennett LD. Ophthalmic Genet. 2021 Feb; 42(1):15-22. Epub 2020 Oct 14.

RefSeq genomic sequence
See the genomic reference sequence for the CNGB1 gene (NG_016351.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the CNGB1 gene.

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Q14028 [Domain Mapping of Disease Mut...]
Q14028
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein