Hs06173338_cn

• Gene Symbol: PHF20L1
• Assay Reference Genome Location: Chr.8:132781855 on build GRCh38
• Cytoband: 8q24.22

Target Gene Details

• Entrez Gene ID: 51105
• Gene Name: PHD finger protein 20-like 1
• Gene Aliases: CGI-72, TDRD20B, URLC1
• Location: Chr.8:132775358-132848807 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PHF20L1	NM_001277196.1			NP_001264125.1
	NM_016018.4			NP_057102.4
	NM_198513.1			NP_940915.1
	XM_005250931.1			XP_005250988.1
	XM_011517075.1			XP_011515377.1
	XM_011517076.1			XP_011515378.1
	XM_011517077.1			XP_011515379.1
	XM_011517078.1			XP_011515380.1
	XM_011517079.1			XP_011515381.1
	XM_011517080.1			XP_011515382.1
	XM_011517081.1			XP_011515383.1
	XM_011517088.1			XP_011515390.1
	XM_017013509.1			XP_016868998.1
	XM_017013510.1			XP_016868999.1
	XM_017013511.1			XP_016869000.1
	XM_017013512.1			XP_016869001.1
	XM_017013513.1			XP_016869002.1
	XM_017013514.1			XP_016869003.1
	XM_017013516.1			XP_016869005.1
	XM_017013517.1			XP_016869006.1
	AB101203.1
	AK022280.1
	AK290506.1
	AL538135.3
	BC015211.1			AAH15211.1
	CD557358.1
	DB498348.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv831463	Chr.8:132723206 - 132905755 on Build GRCh38	Gain	TMEM71 TG PHF20L1
nsv1016348	Chr.8:132769270 - 132803626 on Build GRCh38	Loss	PHF20L1
dgv7317n100	Chr.8:132769940 - 132833582 on Build GRCh38	Loss	PHF20L1

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

protein binding
metal ion binding