Hs03686012_cn

• Gene Symbol: SLC39A14
• Assay Reference Genome Location: Chr.8:22369589 on build GRCh38
• Cytoband: 8p21.3

Target Gene Details

• Entrez Gene ID: 23516
• Gene Name: solute carrier family 39 member 14
• Gene Aliases: HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19
• Location: Chr.8:22367249-22434129 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC39A14	NM_001128431.2			NP_001121903.1
	NM_001135153.1			NP_001128625.1
	NM_001135154.1			NP_001128626.1
	NM_015359.4			NP_056174.2
	XM_005273465.2			XP_005273522.1
	XM_006716323.2			XP_006716386.1
	XM_006716324.2			XP_006716387.1
	XM_011544478.2			XP_011542780.1
	XM_017013292.1			XP_016868781.1
	XM_017013293.1			XP_016868782.1
	XM_017013294.1			XP_016868783.1
	AK172810.1			BAD18780.1
	AK295807.1
	BC015770.1			AAH15770.1
	D31887.1
	DC323208.1
	DC423882.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv6116	Chr.8:22368575 - 22399366 on Build GRCh38	Insertion	SLC39A14
nsv831266	Chr.8:22315953 - 22476033 on Build GRCh38	Loss	PPP3CC SLC39A14 PIWIL2
nsv518646	Chr.8:22296620 - 22520605 on Build GRCh38	Gain	PPP3CC SLC39A14 PIWIL2
esv2764071	Chr.8:22342635 - 22519221 on Build GRCh38	Gain	PPP3CC SLC39A14 PIWIL2
esv2759604	Chr.8:20675533 - 23254096 on Build GRCh38	Loss	LOC101929172 PPP3CC EGR3 NUDT18 CHMP7 GFRA2 CCAR2 HR PEBP4 PHYHIP LOC107984124 LOC107986876 LOC101929237 RHOBTB2 SFTPC TNFRSF10D LGI3 MIR320A SORBS3 LOC286059 XPO7 LOC389641 BIN3 LOC286114 POLR3D SLC39A14 TNFRSF10A DMTN PIWIL2 LOC100507071 LOC102467222 FAM160B2 BIN3-IT1 NPM2 TNFRSF10B REEP4 TNFRSF10C C8orf58 FGF17 LOC254896 DOK2 BMP1 PDLIM2

More Information

Additional Information:

For this assay, SNP(s) [rs79677354] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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

Panther Classification:

Molecular Function -

secondary carrier transporter

Gene Ontology Categories:

Process(es)

cellular zinc ion homeostasis
zinc II ion transmembrane transport
zinc II ion transmembrane import
ferrous iron transmembrane transport

Function(s)

zinc ion transmembrane transporter activity
ferrous iron transmembrane transporter activity