Hs01473457_cn

• Gene Symbol: HMGXB4
• Assay Reference Genome Location: Chr.22:35257531 on build GRCh38
• Cytoband: 22q12.3

Target Gene Details

• Entrez Gene ID: 10042
• Gene Name: HMG-box containing 4
• Gene Aliases: HMG2L1, HMGBCG, THC211630
• Location: Chr.22:35257274-35295807 on Build GRCh38
• Assay Gene Location: Overlaps Exon 1 - Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HMGXB4	NM_001003681.2			NP_001003681.1
	NR_027780.1
	XM_006724100.3			XP_006724163.1
	XM_006724101.3			XP_006724164.1
	XM_006724102.1			XP_006724165.1
	AJ010070.1			CAA08992.1
	AK299833.1
	AL079310.1			CAB45240.1
	BC017326.2			AAH17326.1
	BC052624.1			AAH52624.1
	BC062413.1			AAH62413.1
	CB991207.1
	DW452042.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv588948	Chr.22:35249531 - 35260247 on Build GRCh38	Loss	HMGXB4

More Information

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

Gene Ontology Categories:

Process(es)

endosome to lysosome transport
Wnt signaling pathway
negative regulation of Wnt signaling pathway

Function(s)

DNA binding