SNRPN Products

Antibodies
SNRPN Antibody
SNRPN Antibody
NBP2-20439
Species: Hu, Mu, Rt
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
SNRPN Antibody
SNRPN Antibody
NBP1-74239
Species: Hu
Applications: WB
Host: Rabbit Polyclonal
SNRPN Antibody
SNRPN Antibody
H00006638-B01P
Species: Hu
Applications: WB
Host: Mouse Polyclonal
Lysates
SNRPN Overexpression Lysate ( ...
SNRPN Overexpression Lysate (Denat...
H00006638-T01
Species: Hu
Applications: WB
SNRPN Overexpression Lysate ( ...
SNRPN Overexpression Lysate (Native)
NBL1-16295
Applications: WB
SNRPN Overexpression Lysate ( ...
SNRPN Overexpression Lysate (Native)
NBP2-06402
Applications: WB
Proteins
Recombinant Human SNRPN Prote ...
Recombinant Human SNRPN Protein
H00006638-P01
Species: Hu
Applications: WB, ELISA, PA
Recombinant Human SNRPN Prote ...
Recombinant Human SNRPN Protein
H00006638-P02
Species: Hu
Applications: WB, ELISA, PA
RNAi
SNRPN RNAi
SNRPN RNAi
H00006638-R05
Species: Hu
Applications: RNAi, RNAi SP
SNRPN RNAi
SNRPN RNAi
H00006638-R02
Species: Hu
Applications: RNAi, RNAi SP
SNRPN RNAi
SNRPN RNAi
H00006638-R03
Species: Hu
Applications: RNAi, RNAi SP

Description

The protein encoded by this gene is one polypeptide of a small nuclear ribonucleoprotein complex and belongs to the snRNP SMB/SMN family. The protein plays a role in pre-mRNA processing, possibly tissue-specific alternative splicing events. Although individual snRNPs are believed to recognize specific nucleic acid sequences through RNA-RNA base pairing, the specific role of this family member is unknown. The protein arises from a bicistronic transcript that also encodes a protein identified as the SNRPN upstream reading frame (SNURF). Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5' untranslated region. Additional splice variants have been described but sequences for the complete transcripts have not been determined. The 5' UTR of this gene has been identified as an imprinting center. Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure.

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Human
Human
Human
Human
Human
Human
Product By Gene ID 6638
Alternate Names
  • DKFZp761I1912
  • snRNP-N
  • DKFZp686M12165
  • SmN
  • DKFZp686C0927
  • Sm-N
  • Prader-Willi syndrome chromosome region
  • Sm-D
  • Tissue-specific-splicing protein
  • tissue-specific splicing protein
  • Sm protein N
  • small nuclear ribonucleoprotein-associated protein N
  • Sm protein D
  • sm-N
  • SNURF-SNRPN
  • PWCR
  • SNRNP-N
  • MGC29886
  • SM-D
  • FLJ39265
  • RT-LI
  • SMNFLJ36996
  • HCERN3FLJ33569
  • DKFZp762N022
  • small nuclear ribonucleoprotein polypeptide N

Research Areas for SNRPN

Find related products by research area and learn more about each of the different research areas below.

Diabetes Research

PTMs for SNRPN

Learn more about PTMs related to SNRPN.

Methylation
Demethylation
Acetylation
Deacetylation
Phosphorylation
Cleavage
Reduction

Bioinformatics Tool for SNRPN

Discover related pathways, diseases and genes to SNRPN. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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