Homo sapiens phosphodiesterase 6B (PDE6B), transcript variant 7, mRNA

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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.
The CRL4(DCAF6) E3 ligase ubiquitinates CtBP1/2 to induce apoptotic signalling and promote intervertebral disc degeneration. [J Mol Med (Berl). 2023]
The CRL4(DCAF6) E3 ligase ubiquitinates CtBP1/2 to induce apoptotic signalling and promote intervertebral disc degeneration.
Tseng C, Han Y, Lv Z, Song Q, Wang K, Shen H, Chen Z. J Mol Med (Berl). 2023 Feb; 101(1-2):171-181. Epub 2023 Jan 23.

RefSeq alternative splicing
See 23 reference mRNA sequence splice variants for the PDE6B gene.
RefSeq protein product
See the reference protein sequence for rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta isoform 3 (NP_001366176.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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Nucleotide