NSUN5
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Putative methyltransferase NSUN5 is an enzyme that in humans is encoded by the NSUN5 gene.[1][2][3]
This gene encodes a protein with similarity to p120 (NOL1), a 120-kDa proliferation-associated nucleolar antigen that is a member of an evolutionarily conserved protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in two transcript variants encoding different isoforms.[3]
References
Further reading
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