MeSH Browser

MeSH Supplementary: NSUN5 protein, human
Unique ID: C455826
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C455826
Entry Term(s): NOL1-NOP2-Sun domain family, member 5 protein, human; WBSCR20A protein, human; Williams Beuren syndrome chromosome region 20A protein, human
Registry Numbers: EC 2.1.1.-
Heading Mapped to: *Methyltransferases; *Muscle Proteins
Frequency: 6
Note: RefSeq NM_148956
Source: Cytogenet Cell Genet 2001;95(1-2):20-7
Indexing Information: Williams Syndrome
Date of Entry: 2002/06/05
Revision Date: 2007/05/14

NSUN5 protein, human MeSH Supplementary Concept Data 2025