rod cGMP phosphodiesterase delta subunit [Homo sapiens]

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A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22). [Eur J Med Genet. 2019]
A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22).
Mégarbané A, Hmaimess G, Bizzari S, El-Bazzal L, Al-Ali MT, Stora S, Delague V, El-Hayek S. Eur J Med Genet. 2019 Nov; 62(11):103576. Epub 2018 Nov 10.
Prenylation defects in inherited retinal diseases. [J Med Genet. 2014]
Prenylation defects in inherited retinal diseases.
Roosing S, Collin RW, den Hollander AI, Cremers FP, Siemiatkowska AM. J Med Genet. 2014 Mar; 51(3):143-51. Epub 2014 Jan 8.
Identification of PDE6D as a molecular target of anecortave acetate via a methotrexate-anchored yeast three-hybrid screen. [ACS Chem Biol. 2013]
Identification of PDE6D as a molecular target of anecortave acetate via a methotrexate-anchored yeast three-hybrid screen.
Shepard AR, Conrow RE, Pang IH, Jacobson N, Rezwan M, Rutschmann K, Auerbach D, Sriramaratnam R, Cornish VW. ACS Chem Biol. 2013 Mar 15; 8(3):549-58. Epub 2013 Jan 9.

RefSeq genomic sequence
See the genomic reference sequence for the PDE6D gene (NG_034064.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the PDE6D gene.

Nucleotide
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein