rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta isoform - Protein

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A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA Splicing. [Ophthalmic Res. 2023]
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA Splicing.
Ullah M, Rehman AU, Folcher M, Ullah A, Usman F, Rashid A, Khan B, Quinodoz M, Ansar M, Rivolta C. Ophthalmic Res. 2023; 66(1):878-884. Epub 2023 Apr 24.
A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family. [BMC Ophthalmol. 2023]
A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.
Aziz N, Ullah M, Rashid A, Hussain Z, Shah K, Awan A, Khan M, Ullah I, Rehman AU. BMC Ophthalmol. 2023 Mar 23; 23(1):116. Epub 2023 Mar 23.
Identification of a novel large multigene deletion and a frameshift indel in PDE6B as the underlying cause of early-onset recessive rod-cone degeneration. [Cold Spring Harb Mol Case Stud...]
Identification of a novel large multigene deletion and a frameshift indel in PDE6B as the underlying cause of early-onset recessive rod-cone degeneration.
Sangermano R, Biswas P, Sullivan LS, Place EM, Borooah S, Straubhaar J, Pierce EA, Daiger SP, Bujakowska KM, Ayaggari R. Cold Spring Harb Mol Case Stud. 2022 Dec; 8(7). Epub 2022 Dec 28.

RefSeq genomic sequence
See the genomic reference sequence for the PDE6B gene (NG_009839.2).
RefSeq mRNA
See reference mRNA sequence for the PDE6B gene (NM_001350155.3).

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Protein