RecName: Full=Heterogeneous nuclear ribonucleoprotein Q; Short=hnRNP Q - Protein

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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 genomic sequence
See the genomic reference sequence for the SYNCRIP gene (NG_031848.1).
RefSeq protein isoforms
See 26 reference sequence protein isoforms for the SYNCRIP gene.

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O60506 [Domain Mapping of Disease Mut...]
O60506
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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reagent reviews [ExactAntigen/Labome]
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reagents [ExactAntigen/Labome]
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RecName: Full=Heterogeneous nuclear ribonucleoprotein Q; Short=hnRNP Q; AltName:...
RecName: Full=Heterogeneous nuclear ribonucleoprotein Q; Short=hnRNP Q; AltName: Full=Glycine- and tyrosine-rich RNA-binding protein; Short=GRY-RBP; AltName: Full=NS1-associated protein 1; AltName: Full=Synaptotagmin-binding, cytoplasmic RNA-interacting protein
gi|92090361|sp|O60506.2|HNRPQ_HUMAN

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