Hs01012919_cn

• Gene Symbol: MTUS1
• Assay Reference Genome Location: Chr.8:17644923 on build GRCh38
• Cytoband: 8p22

Target Gene Details

• Entrez Gene ID: 57509
• Gene Name: microtubule associated tumor suppressor 1
• Gene Aliases: ATBP, ATIP, ICIS, MP44, MTSG1
• Location: Chr.8:17643794-17801579 on Build GRCh38
• Assay Gene Location: Within Exon 26

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MTUS1	NM_001001924.2	15	5290	NP_001001924.1
	NM_001001925.2	14	5128	NP_001001925.1
	NM_001001931.2	12	2877	NP_001001931.1
	NM_001166393.1	12	2522	NP_001159865.1
	NM_020749.4	10	2674	NP_065800.1
	XM_005273577.3	15	5198	XP_005273634.1
	XM_005273578.3	15	5286	XP_005273635.1
	XM_005273579.3	15	5202	XP_005273636.1
	XM_005273580.3	14	5036	XP_005273637.1
	XM_005273581.3	14	5124	XP_005273638.1
	XM_005273582.3	14	5040	XP_005273639.1
	XM_011544595.2	15	5232	XP_011542897.1
	XM_017013698.1	16	5204	XP_016869187.1
	XM_017013699.1	16	5426	XP_016869188.1
	XM_017013700.1	15	5089	XP_016869189.1
	XM_017013701.1	16	5206	XP_016869190.1
	XM_017013702.1	14	4861	XP_016869191.1
	XM_017013704.1	9	2196	XP_016869193.1
	AB033114.1	14	4742	BAA86602.1
	AF121259.1	10	2314	AAG33674.1
	AF394227.1	1	1011
	AK000172.1	3	1415
	AK024357.1	9	2200	BAB14894.1
	AK026661.1	1	788
	AK125188.1	12	2877
	AL096842.1	15	4082	CAB50791.1
	BC033842.1	7	1766	AAH33842.1
	BC136320.1	15	5041
	BC142971.1	10	2607
	BX648879.1	8	3180	CAH56128.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2764066	Chr.8:17530064 - 17677066 on Build GRCh38	Gain+Loss	MTUS1 PDGFRL SLC7A2
esv3616489	Chr.8:17490020 - 17737549 on Build GRCh38	Loss	MTUS1 PDGFRL SLC7A2 MIR548V
nsv831247	Chr.8:17541589 - 17701918 on Build GRCh38	Gain	MTUS1 PDGFRL SLC7A2 MIR548V
esv3616492	Chr.8:17598147 - 17735569 on Build GRCh38	Loss	MTUS1 PDGFRL MIR548V
nsv831249	Chr.8:17644116 - 17838769 on Build GRCh38	Loss	MTUS1 MIR548V
esv34867	Chr.8:17488520 - 17725642 on Build GRCh38	Loss	MTUS1 PDGFRL SLC7A2 MIR548V
esv3891364	Chr.8:17633635 - 17678837 on Build GRCh38	Gain	MTUS1 PDGFRL
esv2759600	Chr.8:17433671 - 17784021 on Build GRCh38	Loss	MTUS1 PDGFRL SLC7A2 MIR548V

More Information

Additional Information:

For this assay, SNP(s) [rs73668803] 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, Exonic, DGV Variation