Hs03539694_cn

• Gene Symbol: FAM53A
• Assay Reference Genome Location: Chr.4:1604388 on build GRCh38
• Cytoband: 4p16.3

Target Gene Details

• Entrez Gene ID: 152877
• Gene Name: family with sequence similarity 53 member A
• Gene Aliases: DNTNP
• Location: Chr.4:1574055-1684313 on Build GRCh38
• Assay Gene Location: Within Intron 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM53A	XM_011513404.2			XP_011511706.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv8900n54	Chr.4:1601262 - 1625429 on Build GRCh38	Gain	FAM53A
dgv8897n54	Chr.4:1532249 - 1617803 on Build GRCh38	Loss	FAM53A
nsv593316	Chr.4:1526039 - 1768630 on Build GRCh38	Gain	SLBP FAM53A TACC3 TMEM129
nsv949753	Chr.4:1532074 - 1630173 on Build GRCh38	Deletion	FAM53A
nsv593322	Chr.4:1589655 - 1622987 on Build GRCh38	Gain	FAM53A
nsv470000	Chr.4:1522203 - 1722852 on Build GRCh38	Loss	SLBP FAM53A TACC3 TMEM129
nsv593320	Chr.4:1553021 - 1657401 on Build GRCh38	Loss	FAM53A

More Information

Additional Information:

For this assay, SNP(s) [rs115411187] 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