Hs07223816_cn

• Gene Symbol: HSPA12B
• Assay Reference Genome Location: Chr.20:3736407 on build GRCh38
• Cytoband: 20p13

Target Gene Details

• Entrez Gene ID: 116835
• Gene Name: heat shock protein family A (Hsp70) member 12B
• Gene Aliases: C20orf60
• Location: Chr.20:3732670-3753111 on Build GRCh38
• Assay Gene Location: Overlaps Intron 1 - Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HSPA12B	NM_001197327.1			NP_001184256.1
	NM_001318322.1			NP_001305251.1
	NM_052970.4			NP_443202.3
	XM_017027632.1			XP_016883121.1
	XM_017027633.1			XP_016883122.1
	XM_017027634.1			XP_016883123.1
	XM_017027635.1			XP_016883124.1
	AK056712.1			BAB71261.1
	AK297120.1
	AK301294.1
	BC090857.1			AAH90857.1
	BC110881.1			AAI10882.1
	BC117284.1
	BC126263.1
	BC143932.1
	CB990660.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833899	Chr.20:3709295 - 3878350 on Build GRCh38	Loss	SPEF1 MAVS HSPA12B CDC25B SIGLEC1 AP5S1 C20orf27 CENPB LOC101929125
nsv470536	Chr.20:3693168 - 3747379 on Build GRCh38	Loss	HSPA12B SIGLEC1
esv3575355	Chr.20:3667953 - 3752840 on Build GRCh38	Gain	ADAM33 HSPA12B SIGLEC1
nsv585284	Chr.20:3705789 - 3756848 on Build GRCh38	Loss	HSPA12B SIGLEC1 C20orf27
nsv520565	Chr.20:3652593 - 3740054 on Build GRCh38	Loss	ADAM33 HSPA12B SIGLEC1 GFRA4
esv3645047	Chr.20:3734083 - 3737371 on Build GRCh38	Loss	HSPA12B

More Information

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

Gene Ontology Categories:

Function(s)

protein binding
ATP binding