heterogeneous nuclear ribonucleoprotein Q isoform X3 [Bos taurus]

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Oculopharyngeal muscular dystrophy mutations link the RNA-binding protein HNRNPQ to autophagosome biogenesis. [Aging Cell. 2023]
Oculopharyngeal muscular dystrophy mutations link the RNA-binding protein HNRNPQ to autophagosome biogenesis.
Ishtayeh H, Galves M, Barnatan TT, Berdichevsky Y, Amer-Sarsour F, Pasmanik-Chor M, Braverman I, Blumen SC, Ashkenazi A. Aging Cell. 2023 Oct; 22(10):e13949. Epub 2023 Aug 9.
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder. [Hum Mutat. 2021]
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder.
Semino F, Schröter J, Willemsen MH, Bast T, Biskup S, Beck-Woedl S, Brennenstuhl H, Schaaf CP, Kölker S, Hoffmann GF, et al. Hum Mutat. 2021 Sep; 42(9):1094-1100. Epub 2021 Jul 5.
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. [Genome Med. 2021]
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, et al. Genome Med. 2021 Apr 19; 13(1):63. Epub 2021 Apr 19.

RefSeq mRNA
See reference mRNA sequence for the SYNCRIP gene (XM_024996982.2).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the SYNCRIP gene.

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Protein