nonsense-mediated mRNA decay factor SMG9 isoform X1 [Homo sapiens]

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Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing. [BMC Med Genomics. 2022]
Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing.
Yang Q, Qin Z, Zhang Q, Yi S, Yi S, Luo J. BMC Med Genomics. 2022 Mar 23; 15(1):67. Epub 2022 Mar 23.
A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development. [Eur J Hum Genet. 2022]
A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development.
Rahikkala E, Urpa L, Ghimire B, Topa H, Kurki MI, Koskela M, Airavaara M, Hämäläinen E, Pylkäs K, Körkkö J, et al. Eur J Hum Genet. 2022 May; 30(5):619-627. Epub 2022 Jan 28.
Further delineation of SMG9-related heart and brain malformation syndrome. [Am J Med Genet A. 2021]
Further delineation of SMG9-related heart and brain malformation syndrome.
Altuwaijri N, Abdelbaky M, Alhashem A, Alrakaf M, Hashem M, Alzahrani F, Alkuraya FS. Am J Med Genet A. 2021 May; 185(5):1624-1630. Epub 2021 Feb 20.

RefSeq genomic sequence
See the genomic reference sequence for the SMG9 gene (NG_051200.1).
RefSeq mRNA
See reference mRNA sequence for the SMG9 gene (XM_011527113.2).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the SMG9 gene.

nonsense-mediated mRNA decay factor SMG9 isoform X1 [Homo sapiens]
nonsense-mediated mRNA decay factor SMG9 isoform X1 [Homo sapiens]
gi|768009995|ref|XP_011525415.1|

Protein
Homo sapiens RPL34 divergent transcript (RPL34-DT), long non-coding RNA
Homo sapiens RPL34 divergent transcript (RPL34-DT), long non-coding RNA
gi|224028263|ref|NR_026968.1|

Nucleotide

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Protein