Name

NSUN5 Gene

NOP2/Sun domain family, member 5

This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]

NSUN5P2 Gene

NOP2/Sun domain family, member 5 pseudogene 2

This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [provided by RefSeq, Jul 2013]

NSUN5P1 Gene

NOP2/Sun domain family, member 5 pseudogene 1

This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

NSUN5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for NSUN5 from the Pathway Commons Protein-Protein Interactions dataset.

NSUN5P1 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for NSUN5P1 from the NURSA Protein-Protein Interactions dataset.