Gene: [11p155/BWSCR1A] Beckwith-Wiedemann syndrome chromosome region 1, candidate a; imprinted polyspecific membrane transporter 1; organic cation transporter-like 2; solute carrier family 22, member 1-like; [BWR1A IMPT1 ]

REL	GEM:11p155/BWSCR1B; GEM:11p155/CDKN1C
REF	COD,SEQ "Cooper PR &: Genomics, 49, 38-51, 1998 COD,SEQ "Dao D &: Hum Mol Genet, 7, 597-608, 1998 COD,SEQ "Morisaki H &: DNA Res, 5, 235-240, 1998 COD,SEQ "Reece M &: FEBS Lett, 433, 245-250, 1998 COD,SEQ,LOC,FAG "Schwienbacher C &: PNAS, 95, 3873-3878, 1998
KEY	ion, trp
CLA	coding, basic
LOC	11 p15.5
MIM	MIM: 602631
SYN	BWR1A IMPT1