Hs04444007_cn

• Gene Symbol: DMXL2
• Assay Reference Genome Location: Chr.15:51469886 on build GRCh38
• Cytoband: 15q21.2

Target Gene Details

• Entrez Gene ID: 23312
• Gene Name: Dmx like 2
• Gene Aliases: PEPNS, RC3
• Location: Chr.15:51447724-51622833 on Build GRCh38
• Assay Gene Location: Within Intron 31

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
DMXL2	NM_001174116.1			NP_001167587.1
	NM_001174117.1			NP_001167588.1
	NM_015263.3			NP_056078.2
	XM_005254255.1			XP_005254312.1
	XM_005254256.1			XP_005254313.1
	XM_017022034.1			XP_016877523.1
	AB020663.2			BAA74879.2
	AF389880.1			AAL93215.1
	BC140781.1
	BC144539.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3636461	Chr.15:51022583 - 51482654 on Build GRCh38	Gain	MIR7973-2 DMXL2 GLDN CYP19A1 MIR7973-1 PIRC66 TNFAIP8L3 MIR4713
nsv471243	Chr.15:51053288 - 51725899 on Build GRCh38	Gain	MIR7973-2 DMXL2 GLDN CYP19A1 MIR7973-1 SCG3 PIRC66 TNFAIP8L3 MIR4713 LYSMD2
esv2760031	Chr.15:50990060 - 51538142 on Build GRCh38	Gain	MIR7973-2 DMXL2 AP4E1 GLDN CYP19A1 MIR7973-1 PIRC66 TNFAIP8L3 MIR4713
dgv4526n54	Chr.15:50582767 - 51475068 on Build GRCh38	Gain	MIR7973-2 DMXL2 AP4E1 SPPL2A GLDN CYP19A1 MIR7973-1 TRPM7 PIRC66 TNFAIP8L3 MIR4713 DCAF13P3

More Information

Additional Information:

For this assay, SNP(s) [rs148892493] 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

Gene Ontology Categories:

Function(s)

Rab GTPase binding