Homo sapiens phosphodiesterase 10A (PDE10A), transcript variant 2, mRN - Nucleotide

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PDE10A Mutation as an Emerging Cause of Childhood-Onset Hyperkinetic Movement Disorders: A Review of All Published Cases. [Neuropediatrics. 2024]
PDE10A Mutation as an Emerging Cause of Childhood-Onset Hyperkinetic Movement Disorders: A Review of All Published Cases.
Kalampokini S, Xiromerisiou G, Bargiotas P, Anastasiadou VC, Costeas P, Hadjigeorgiou GM. Neuropediatrics. 2024 Aug; 55(4):217-223. Epub 2024 Mar 5.
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders. [Parkinsonism Relat Disord. 2023]
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders.
Bohlega S, Abusrair AH, Al-Qahtani Z, Guzmán-Vega FJ, Ramakrishnan R, Aldosari H, Aldakheel A, Al-Qahtani S, Monies D, Arold ST. Parkinsonism Relat Disord. 2023 Mar; 108:105323. Epub 2023 Feb 13.
Phosphodiesterase 10A (PDE10A) as a novel target to suppress β-catenin and RAS signaling in epithelial ovarian cancer. [J Ovarian Res. 2022]
Phosphodiesterase 10A (PDE10A) as a novel target to suppress β-catenin and RAS signaling in epithelial ovarian cancer.
Borneman RM, Gavin E, Musiyenko A, Richter W, Lee KJ, Crossman DK, Andrews JF, Wilhite AM, McClellan S, Aragon I, et al. J Ovarian Res. 2022 Nov 2; 15(1):120. Epub 2022 Nov 2.

RefSeq alternative splicing
See 20 reference mRNA sequence splice variants for the PDE10A gene.
RefSeq protein product
See the reference protein sequence for cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A isoform 2 (NP_006652.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens phosphodiesterase 10A (PDE10A), transcript variant 2, mRNA
Homo sapiens phosphodiesterase 10A (PDE10A), transcript variant 2, mRNA
gi|1677500833|ref|NM_006661.4|

Nucleotide
Striatal degeneration, autosomal dominant 2
Striatal degeneration, autosomal dominant 2

MedGen
C4310791[conceptid] (1)
MedGen

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Nucleotide