Hs05343858_cn

• Gene Symbol: TMEM266
• Assay Reference Genome Location: Chr.15:76077311 on build GRCh38
• Cytoband: 15q24.2

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 1

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
	AK056777.1
	AK095509.1			BAC04562.1
	AK308676.1
	DA090797.1
	DA483185.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2749895	Chr.15:75415580 - 76472296 on Build GRCh38	Deletion	DNM1P35 TYRO3P LOC107984799 FBXO22 LOC101929439 IMP3 FBXO22-AS1 SNUPN ETFA TMEM266 UBE2Q2 NRG4 SIN3A CSPG4 SNX33 MIR4313 SCAPER PTPN9 LOC441728 ISL2 ODF3L1
nsv1048760	Chr.15:76042203 - 76204636 on Build GRCh38	Gain	TMEM266 LOC101929439 NRG4
nsv569998	Chr.15:75940264 - 76258597 on Build GRCh38	Gain	TMEM266 LOC101929439 NRG4 ETFA
esv2669418	Chr.15:76073911 - 76078466 on Build GRCh38	Deletion	TMEM266
nsv833057	Chr.15:76075507 - 76293527 on Build GRCh38	Loss	TYRO3P TMEM266 LOC101929439 ETFA
esv3636935	Chr.15:76073935 - 76078476 on Build GRCh38	Loss	TMEM266
esv2749898	Chr.15:75764003 - 77933523 on Build GRCh38	Deletion	TYRO3P LINGO1-AS2 LOC101929457 FBXO22 LINGO1-AS1 LOC101929439 FBXO22-AS1 TSPAN3 ETFA RCN2 MIR3713 TMEM266 LINC00597 UBE2Q2 LINGO1 LOC645752 PSTPIP1 NRG4 SCAPER LOC441728 PEAK1 ISL2 HMG20A

More Information

Additional Information:

For this assay, SNP(s) [rs76631432] 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