Hs07029411_cn

• Gene Symbol: SUGT1
• Assay Reference Genome Location: Chr.13:52678337 on build GRCh38
• Cytoband: 13q14.3

Target Gene Details

• Entrez Gene ID: 10910
• Gene Name: SGT1 homolog, MIS12 kinetochore complex assembly cochaperone
• Gene Aliases: SGT1
• Location: Chr.13:52652691-52700756 on Build GRCh38
• Assay Gene Location: Within Intron 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SUGT1	NM_001130912.2			NP_001124384.1
	NM_001320831.1			NP_001307760.1
	NM_006704.4			NP_006695.1
	XM_011534891.2			XP_011533193.1
	XM_011534893.2			XP_011533195.1
	XM_017020365.1			XP_016875854.1
	XM_017020366.1			XP_016875855.1
	XM_017020367.1			XP_016875856.1
	XM_017020368.1			XP_016875857.1
	AF132856.1			AAD30062.1
	AJ344097.1			CAC51433.1
	AK291402.1
	AK292128.1
	AK302363.1
	AY271314.1			AAQ01749.1
	AY321358.1			AAQ76039.1
	BC000911.1			AAH00911.1
	BT009798.1			AAP88800.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1044949	Chr.13:52497005 - 52715291 on Build GRCh38	Gain	TPTE2P3 LECT1 SUGT1 HNRNPA1L2
dgv1653n100	Chr.13:52564997 - 52728939 on Build GRCh38	Gain	TPTE2P3 LECT1 SUGT1 HNRNPA1L2
nsv820041	Chr.13:52487203 - 52706453 on Build GRCh38	Gain	TPTE2P3 LECT1 SUGT1 HNRNPA1L2

More Information

Additional Information:

For this assay, SNP(s) [rs143650225] 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:

Process(es)

mitotic nuclear division
regulation of protein stability
positive regulation by host of symbiont catalytic activity

Function(s)

protein binding