ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Gene Report

Basic Info
Approved Symbol SNRPN
Previous Symbol PWCR
Symbol Alias SMN, SM-D, HCERN3, SNRNP-N, SNURF-SNRPN, RT-LI
Approved Name small nuclear ribonucleoprotein polypeptide N
Previous Name Prader-Willi syndrome chromosome region
Name Alias tissue-specific splicing protein, "SM protein N", "small nuclear ribonucleoprotein N"
Location 15q12
Position chr15:25068794-25664609, +
External Links HGNC: 11164
Entrez Gene: 6638
Ensembl: ENSG00000128739
UCSC: uc001ywt.1
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source Mapped by CNV; Mapped by PBA pathway; Mapped by significant region

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 1)

Gene related other variant (count: 0)

Gene related regions (count: 1)

Gene related GO terms (count: 8)

GO terms by PBA (with statistical significance of FDR<0.05) (count: 1)

GO terms by database search (count: 7)


Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with SNRPN (count: 3)

Genes shared at least 2 KEGG pathways with SNRPN (count: 0)

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Region: chr15:25068794..25664609 View in gBrowse
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