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SNRPN gene

Known as: small nuclear ribonucleoprotein N, tissue-specific splicing protein, SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N 
This gene plays a role in splicing of mRNA.
National Institutes of Health

Related topics

Related topics

3 relations
RNA SplicingSNRPD3 genesmall nuclear ribonucleoprotein-associated protein N

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Aberrant DNA Methylation of IGF2-H19 Locus in Human Fetus and in Spermatozoa From Assisted Reproductive Technologies
Given the higher risk of developing imprinting disorders in assisted reproductive technology (ART)-conceived children, we… 
2018
2018
Mild SMN missense alleles are only functional in the presence of SMN2 in mammals
Spinal muscular atrophy (SMA) is caused by reduced levels of full-length SMN (FL-SMN). In SMA patients with one or two copies of… 
2007
2007
High-resolution melting for accurate assessment of DNA methylation.
Methylation of cytosine in DNA is an epigenetic mark that is important for genome stability, transcriptional regulation of… 
2007
2007
Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter
AbstractPrader-Willi syndrome (PWS) is a neurodevelopmental disorder associated with abnormalities of chromosome 15q11q13. The… 
2007
2007
Effect of sample aliquot size on the limit of detection and reproducibility of clinical assays.
BACKGROUND Nucleic acid amplification technologies significantly improved the limit of detection (LOD) for diagnostic assays. The… 
Review
2004
Review
2004
Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
Highly Cited
1999
Highly Cited
1999
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC…
Imprinting of the Prader-Willi/Angelman syndrome region on human chromosome 15 is regulated by an imprinting centre (IC), which… 
Highly Cited
1999
Highly Cited
1999
In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.
Human chromosome region 15q11-q13 contains a cluster of oppositely imprinted genes. Loss of the paternal or the maternal alleles… 
1997
1997
Identification of novel exons 3' to the human SNRPN gene.
The gene for the small nuclear ribonucleoprotein N (SNRPN) maps to human chromosome 15 and has 10 exons. Using cDNA cloning… 
1995
1995
Ubiquitous expression and imprinting of Snrpn in the mouse
Snrpn is known to be abundantly expressed in rodent brain and heart, and in two separate studies with neonatal mouse brain it has… 
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