Homo sapiens snurportin 1 (SNUPN), transcript variant 2, mRNA

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SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation. [Nat Commun. 2024]
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.
Nashabat M, Nabavizadeh N, Saraçoğlu HP, Sarıbaş B, Avcı Ş, Börklü E, Beillard E, Yılmaz E, Uygur SE, Kayhan CK, et al. Nat Commun. 2024 Feb 27; 15(1):1758. Epub 2024 Feb 27.
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. [Nat Commun. 2022]
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.
Havugimana PC, Goel RK, Phanse S, Youssef A, Padhorny D, Kotelnikov S, Kozakov D, Emili A. Nat Commun. 2022 Jul 13; 13(1):4043. Epub 2022 Jul 13.
OpenCell: Endogenous tagging for the cartography of human cellular organization. [Science. 2022]
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Cho NH, Cheveralls KC, Brunner AD, Kim K, Michaelis AC, Raghavan P, Kobayashi H, Savy L, Li JY, Canaj H, et al. Science. 2022 Mar 11; 375(6585):eabi6983. Epub 2022 Mar 11.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the SNUPN gene.
RefSeq protein product
See the reference protein sequence for snurportin-1 (NP_001036046.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
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Components (Core)
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Functional Class
Functional class of the sequence domain architecture
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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