MeSH Browser

MeSH Supplementary: SLC22A18 protein, human
Unique ID: C111653
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C111653
Entry Term(s): BWR1A protein, human; Beckwith-Wiedemann syndrome chromosome region 1, candidate a protein, human; IMPT1 protein, human; ORCTL2 protein, human; SLC22A1L protein, human; solute carrier family 22 (organic cation transporter), member 1-like protein, human; solute carrier family 22 (organic cation transporter), member 18 protein, human
Registry Numbers: 0
Previous Indexing: *PROTEINS (1998-2002)
Heading Mapped to: *Organic Cation Transport Proteins
Frequency: 30
Note: RefSeq NM_183233
Source: Proc Natl Acad Sci U S A 1998 Mar 31;95(7):3873-8
Date of Entry: 1998/04/30
Revision Date: 2006/11/02

SLC22A18 protein, human MeSH Supplementary Concept Data 2025