Hs05753852_cn

• Gene Symbol: TMCO4
• Assay Reference Genome Location: Chr.1:19702917 on build GRCh38
• Cytoband: 1p36.13

Target Gene Details

• Entrez Gene ID: 255104
• Gene Name: transmembrane and coiled-coil domains 4
• Gene Aliases: -
• Location: Chr.1:19682213-19800385 on Build GRCh38
• Assay Gene Location: Within Intron 18

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMCO4	NM_181719.4			NP_859070.3
	XM_005245822.4			XP_005245879.1
	XM_005245824.4			XP_005245881.1
	XM_005245825.4			XP_005245882.1
	XM_005245827.3			XP_005245884.1
	XM_006710551.3			XP_006710614.1
	XM_011541179.2			XP_011539481.1
	XM_011541180.2			XP_011539482.1
	XM_011541181.1			XP_011539483.1
	XM_011541185.2			XP_011539487.1
	XM_011541186.2			XP_011539488.1
	XM_017000913.1			XP_016856402.1
	XM_017000914.1			XP_016856403.1
	XM_017000915.1			XP_016856404.1
	XM_017000916.1			XP_016856405.1
	XM_017000917.1			XP_016856406.1
	XM_017000918.1			XP_016856407.1
	XM_017000919.1			XP_016856408.1
	XM_017000920.1			XP_016856409.1
	XM_017000921.1			XP_016856410.1
	XM_017000922.1			XP_016856411.1
	AK127543.1			BAC87027.1
	AL832390.1
	AX775873.1			CAE11636.1
	AX775875.1			CAE11637.1
	AX775877.1			CAE11638.1
	BC053600.1			AAH53600.1
	BX640987.1			CAE45994.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv508991	Chr.1:19567574 - 19705911 on Build GRCh38	Insertion	NBL1 TMCO4 HTR6 RPS14P3 MINOS1-NBL1 MINOS1 LOC105378614
esv3585406	Chr.1:19702531 - 19713294 on Build GRCh38	Loss	TMCO4

More Information

Additional Information:

For this assay, SNP(s) [rs79839140] 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