Hs03980602_cn

• Gene Symbol: SLFN5
• Assay Reference Genome Location: Chr.17:35255530 on build GRCh38
• Cytoband: 17q12

Target Gene Details

• Entrez Gene ID: 162394
• Gene Name: schlafen family member 5
• Gene Aliases: -
• Location: Chr.17:35243026-35273650 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLFN5	NM_144975.3			NP_659412.3
	XM_005257934.3			XP_005257991.1
	AK054668.1			BAB70788.1
	AK303299.1
	AK303632.1
	BC021238.1			AAH21238.1
	BP281007.1
	BX647942.1
	CD704489.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3640444	Chr.17:35250248 - 35255692 on Build GRCh38	Loss	SLFN5
esv2422399	Chr.17:35212221 - 35291582 on Build GRCh38	Deletion	SLFN5 LOC105371932
esv3892998	Chr.17:35106468 - 35295755 on Build GRCh38	Loss	SLFN5 RAD51D UNC45B NLE1 RAD51L3-RFFL SLC35G3 FNDC8 LOC105371932
esv3892999	Chr.17:35252863 - 35925533 on Build GRCh38	Loss	TAF15 SLFN12L SLFN5 PEX12 C17orf50 SLFN14 SLFN11 SNORD7 MMP28 GAS2L2 RDM1 LOC105371743 SLFN12 AP2B1 RASL10B HEATR9 CCL5 LRRC37A8P LOC105371933 SLFN13
nsv574741	Chr.17:35225256 - 35500115 on Build GRCh38	Loss	SLFN12 SLFN12L SLFN5 SLFN11 LOC105371933 LOC105371932 SLFN13

More Information

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

Gene Ontology Categories:

Process(es)

cell differentiation

Function(s)

ATP binding