SNW1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

SNW domain-containing protein 1 is a protein that in humans is encoded by the SNW1 gene.[5][6][7]

AliasesSNW1, Bx42, NCOA-62, PRPF45, Prp45, SKIIP, SKIP, SNW domain containing 1, SKIP1, FUN20
End77,761,207 bp[1]
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SNW1
Identifiers
AliasesSNW1, Bx42, NCOA-62, PRPF45, Prp45, SKIIP, SKIP, SNW domain containing 1, SKIP1, FUN20
External IDsOMIM: 603055; MGI: 1913604; HomoloGene: 56557; GeneCards: SNW1; OMA:SNW1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012245
NM_001318844

NM_025507

RefSeq (protein)

NP_001305773
NP_036377

NP_079783

Location (UCSC)Chr 14: 77.72 – 77.76 MbChr 12: 87.5 – 87.52 Mb
PubMed search[3][4]
Wikidata
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Function

This gene, a member of the SNW gene family, encodes a coactivator that enhances transcription from some Pol II promoters. This coactivator can bind to the ligand-binding domain of the vitamin D receptor and to retinoid receptors to enhance vitamin D-, retinoic acid-, estrogen-, and glucocorticoid-mediated gene expression. It can also function as a splicing factor by interacting with poly(A)-binding protein 2 to directly control the expression of muscle-specific genes at the transcriptional level. Finally, the protein may be involved in oncogenesis since it interacts with a region of SKI oncoproteins that is required for transforming activity.[7]

Interactions

SNW1 has been shown to interact with:

References

Further reading

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