Hs02493822_cn

• Gene Symbol: TTC22
• Assay Reference Genome Location: Chr.1:54784775 on build GRCh38
• Cytoband: 1p32.3

Target Gene Details

• Entrez Gene ID: 55001
• Gene Name: tetratricopeptide repeat domain 22
• Gene Aliases: -
• Location: Chr.1:54779696-54802379 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TTC22	NM_001114108.1			NP_001107580.1
	NM_017904.3	6	1995	NP_060374.2
	XM_011541671.2			XP_011539973.1
	XM_017001582.1			XP_016857071.1
	AI923972.1
	AK000626.1	6	1925	BAA91293.1
	AL049431.1
	AW195337.1	1	206

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv166n100	Chr.1:54741809 - 54804866 on Build GRCh38	Gain	PARS2 TTC22 MROH7-TTC4 TTC4
nsv1000673	Chr.1:54630765 - 54818045 on Build GRCh38	Gain	PARS2 TTC22 MROH7 MROH7-TTC4 LEXM ACOT11 TTC4
nsv546266	Chr.1:54404143 - 54887697 on Build GRCh38	Gain	PARS2 TTC22 MROH7 SSBP3 DHCR24 MROH7-TTC4 FAM151A LEXM ACOT11 TTC4
dgv38e212	Chr.1:54627539 - 54817638 on Build GRCh38	Gain	PARS2 TTC22 MROH7 MROH7-TTC4 LEXM ACOT11 TTC4
nsv817614	Chr.1:54580862 - 55735351 on Build GRCh38	Gain	PARS2 BSND MROH7-TTC4 LEXM ACOT11 LOC100507634 TTC22 MROH7 TMEM61 MIR4422 PCSK9 DHCR24 USP24 FAM151A TTC4

More Information

Additional Information:

For this assay, SNP(s) [rs78948067] 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