[Term] id: PR:Q8N1D0 name: Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (human) def: "A Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q8N1D0] comment: Category=organism-gene. synonym: "hSLC22A18AS" EXACT PRO-short-label [PRO:DNx] synonym: "organic cation transporter-like protein 2 antisense protein (human)" EXACT [UniProtKB:Q8N1D0] synonym: "p27-Beckwith-Wiedemann region 1 B (human)" EXACT [UniProtKB:Q8N1D0] synonym: "p27-BWR1B (human)" EXACT [UniProtKB:Q8N1D0] synonym: "solute carrier family 22 member 1-like antisense protein (human)" EXACT [UniProtKB:Q8N1D0] synonym: "solute carrier family 22 member 18 antisense protein (human)" EXACT [UniProtKB:Q8N1D0] synonym: "BWR1B" RELATED Gene-based [UniProtKB:Q8N1D0] synonym: "BWSCR1B" RELATED Gene-based [UniProtKB:Q8N1D0] synonym: "ORCTL2S" RELATED Gene-based [UniProtKB:Q8N1D0] synonym: "SLC22A18AS" RELATED Gene-based [UniProtKB:Q8N1D0] synonym: "SLC22A1LS" RELATED Gene-based [UniProtKB:Q8N1D0] xref: UniProtKB:Q8N1D0 intersection_of: PR:000014987 ! Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein intersection_of: only_in_taxon NCBITaxon:9606 ! Homo sapiens relationship: has_gene_template HGNC:10965 ! SLC22A18AS (human) relationship: has_canonical_sequence UniProtKB:Q8N1D0 ! Q8N1D0-1