Hs05377569_cn

• Gene Symbol: LOC101929439
• Assay Reference Genome Location: Chr.15:76176664 on build GRCh38
• Cytoband: 15q24.2

Target Gene Details

• Entrez Gene ID: 101929439
• Gene Name: uncharacterized LOC101929439
• Gene Aliases: -
• Location: Chr.15:76174891-76181486 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101929439	NR_120360.1
	AK127738.1

Target Gene Details

• Entrez Gene ID: 123591
• Gene Name: transmembrane protein 266
• Gene Aliases: C15orf27, HVRP1
• Location: Chr.15:76059929-76204963 on Build GRCh38
• Assay Gene Location: Within Intron 10

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMEM266	NM_152335.2			NP_689548.2
	XM_005254160.2			XP_005254217.1
	XM_017021915.1			XP_016877404.1
	XM_017021916.1			XP_016877405.1
	XM_017021917.1			XP_016877406.1
	AK095509.1			BAC04562.1
	AK308676.1
	BC104953.1			AAI04954.1
	BC104955.1			AAI04956.1
	DR007145.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv2625n100	Chr.15:76161853 - 76198206 on Build GRCh38	Gain	LOC101929439 TMEM266
esv2749895	Chr.15:75415580 - 76472296 on Build GRCh38	Deletion	LOC107984799 PTPN9 ISL2 SNUPN LOC101929439 TMEM266 SCAPER ODF3L1 NRG4 FBXO22-AS1 TYRO3P CSPG4 SNX33 IMP3 ETFA UBE2Q2 MIR4313 SIN3A FBXO22 DNM1P35 LOC441728
dgv2623n100	Chr.15:76139033 - 76198206 on Build GRCh38	Gain	LOC101929439 TMEM266
dgv2624n100	Chr.15:76152354 - 76198206 on Build GRCh38	Gain	LOC101929439 TMEM266
nsv1048760	Chr.15:76042203 - 76204636 on Build GRCh38	Gain	NRG4 LOC101929439 TMEM266
nsv569998	Chr.15:75940264 - 76258597 on Build GRCh38	Gain	NRG4 ETFA LOC101929439 TMEM266
nsv833057	Chr.15:76075507 - 76293527 on Build GRCh38	Loss	TYRO3P ETFA LOC101929439 TMEM266
dgv2626n100	Chr.15:76168121 - 76193625 on Build GRCh38	Gain	LOC101929439 TMEM266
esv2749898	Chr.15:75764003 - 77933523 on Build GRCh38	Deletion	MIR3713 ISL2 LOC101929439 LOC645752 TMEM266 TSPAN3 SCAPER LINGO1-AS1 PSTPIP1 NRG4 LINGO1-AS2 LINC00597 FBXO22-AS1 TYRO3P RCN2 ETFA HMG20A UBE2Q2 LOC101929457 PEAK1 FBXO22 LOC441728 LINGO1

More Information

Additional Information:

For this assay, SNP(s) [rs73446471] 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