[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