MeSH Browser

MeSH Supplementary: SLC22A18AS protein, human
Unique ID: C406488
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C406488
Entry Term(s): Beckwith-Wiedemann syndrome chromosome region 1, candidate b protein, human; ORCTL2S protein, human; SLC22A1LS protein, human; organic cation transporter-like 2-antisense protein, human; solute carrier family 22 (organic cation transporter), member 18 antisense protein, human; solute carrier family-22 (organic cation transporter), member 1-like antisense, human
Registry Numbers: 0
Previous Indexing: *CARRIER PROTEINS (1998-2001)
Heading Mapped to: *Membrane Proteins
Frequency: 4
Note: RefSeq NM_007105
Source: Genomics 1998 Apr 1;49(1):38-51
Indexing Information: Beckwith-Wiedemann Syndrome; RNA, Antisense
Date of Entry: 2000/04/14
Revision Date: 2010/08/25

SLC22A18AS protein, human MeSH Supplementary Concept Data 2025