RecName: Full=Heterogeneous nuclear ribonucleoprotein A1; Short=hnRNP - Protein (original) (raw)
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RecName: Full=Heterogeneous nuclear ribonucleoprotein A1; Short=hnRNP A1; AltName: Full=Helix-destabilizing protein; AltName: Full=Single-strand RNA-binding protein; AltName: Full=hnRNP core protein A1; Contains: RecName: Full=Heterogeneous nuclear ribonucleop...
UniProtKB/Swiss-Prot: P09651.5
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Articles about the HNRNPA1 gene
- Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy. [Muscle Nerve. 2024]
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy.
Turner J, Bruels CC, Daugherty AL, Estrella EA, Stafki S, Syeda SB, Littel HR, Pais L, Ganesh VS, Lidov HGW, et al. Muscle Nerve. 2024 Oct; 70(4):843-850. Epub 2024 Jul 28. - Downregulation of HNRNPA1 induced neoantigen generation via regulating alternative splicing. [Mol Med. 2024]
Downregulation of HNRNPA1 induced neoantigen generation via regulating alternative splicing.
Mol Med. 2024 Jun 12; 30(1):85. Epub 2024 Jun 12. - hnRNP A1 dysfunction alters RNA splicing and drives neurodegeneration in multiple sclerosis (MS). [Nat Commun. 2024]
hnRNP A1 dysfunction alters RNA splicing and drives neurodegeneration in multiple sclerosis (MS).
Salapa HE, Thibault PA, Libner CD, Ding Y, Clarke JWE, Denomy C, Hutchinson C, Abidullah HM, Austin Hammond S, Pastushok L, et al. Nat Commun. 2024 Jan 8; 15(1):356. Epub 2024 Jan 8.
More about the HNRNPA1 gene
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PubMed articles cited by protein sequence record - Taxonomy
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LinkOut to external resources
- P09651 [Domain Mapping of Disease Mut...]
P09651
Domain Mapping of Disease Mutations - Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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Finds sub-sequence or patterns in the sequence and highlights the matching region. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences.
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