Hs03771931_cn

• Gene Symbol: SLC22A18AS
• Assay Reference Genome Location: Chr.11:2893934 on build GRCh38
• Cytoband: 11p15.4

Target Gene Details

• Entrez Gene ID: 5003
• Gene Name: solute carrier family 22 member 18 antisense
• Gene Aliases: BWR1B, BWSCR1B, ORCTL2S, SLC22A1LS, p27-BWR1B
• Location: Chr.11:2887344-2905504 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC22A18AS	NM_001302862.1			NP_001289791.1
	NM_007105.3			NP_009036.2
	XM_017017832.1			XP_016873321.1
	XM_017017833.1			XP_016873322.1
	XM_017017834.1			XP_016873323.1
	XM_017017836.1			XP_016873325.1
	AF035407.1			AAC17497.1
	AF037066.1			AAC04789.1
	BC030237.1			AAH30237.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv951292	Chr.11:2792271 - 2927870 on Build GRCh38	Deletion	SLC22A18 SLC22A18AS KCNQ1 CDKN1C KCNQ1-AS1 KCNQ1DN
esv2759795	Chr.11:2767814 - 2942382 on Build GRCh38	Gain	SLC22A18 SLC22A18AS KCNQ1 CDKN1C PHLDA2 KCNQ1-AS1 KCNQ1DN
dgv1575n54	Chr.11:2863338 - 2899436 on Build GRCh38	Loss	SLC22A18AS CDKN1C KCNQ1DN
nsv469930	Chr.11:2831299 - 2924715 on Build GRCh38	Loss	SLC22A18 SLC22A18AS KCNQ1 CDKN1C KCNQ1-AS1 KCNQ1DN
nsv832050	Chr.11:2868540 - 2963987 on Build GRCh38	Loss	NAP1L4 SLC22A18 SLC22A18AS SNORA54 CDKN1C PHLDA2 KCNQ1DN
nsv553111	Chr.11:2842057 - 2904391 on Build GRCh38	Loss	SLC22A18 SLC22A18AS KCNQ1 CDKN1C KCNQ1-AS1 KCNQ1DN
nsv467657	Chr.11:2879188 - 2916401 on Build GRCh38	Loss	SLC22A18 SLC22A18AS CDKN1C

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function