Homo sapiens neurofascin (NFASC), transcript variant 8, mRNA

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A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. [HGG Adv. 2022]
A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors.
Thibord F, Chan MV, Chen MH, Johnson AD. HGG Adv. 2022 Apr 14; 3(2):100095. Epub 2022 Feb 22.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. [Nat Genet. 2021]
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Shelton JF, Shastri AJ, Ye C, Weldon CH, Filshtein-Sonmez T, Coker D, Symons A, Esparza-Gordillo J, 23andMe COVID-19 Team, Aslibekyan S, et al. Nat Genet. 2021 Jun; 53(6):801-808. Epub 2021 Apr 22.
RIG-I regulates myeloid differentiation by promoting TRIM25-mediated ISGylation. [Proc Natl Acad Sci U S A. 2020]
RIG-I regulates myeloid differentiation by promoting TRIM25-mediated ISGylation.
Wu SF, Xia L, Shi XD, Dai YJ, Zhang WN, Zhao JM, Zhang W, Weng XQ, Lu J, Le HY, et al. Proc Natl Acad Sci U S A. 2020 Jun 23; 117(25):14395-14404. Epub 2020 Jun 8.

RefSeq protein product
See the reference protein sequence for neurofascin isoform 8 precursor (NP_001365258.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
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UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Intellectual developmental disorder with speech delay, autism, and dysmorphic fa...
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies

MedGen
X-linked intellectual disability, Cantagrel type
X-linked intellectual disability, Cantagrel type

MedGen

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Nucleotide