Hs03974316_cn

• Gene Symbol: SLFN5
• Assay Reference Genome Location: Chr.17:35254611 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	LOC105371932 SLFN5
esv3892998	Chr.17:35106468 - 35295755 on Build GRCh38	Loss	UNC45B LOC105371932 RAD51D SLC35G3 RAD51L3-RFFL SLFN5 FNDC8 NLE1
esv3892999	Chr.17:35252863 - 35925533 on Build GRCh38	Loss	LOC105371743 SNORD7 SLFN11 SLFN13 GAS2L2 SLFN5 C17orf50 RDM1 SLFN14 HEATR9 LRRC37A8P TAF15 PEX12 MMP28 SLFN12L AP2B1 RASL10B CCL5 LOC105371933 SLFN12
nsv574741	Chr.17:35225256 - 35500115 on Build GRCh38	Loss	SLFN11 LOC105371932 SLFN13 SLFN12L SLFN5 LOC105371933 SLFN12

More Information

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

Gene Ontology Categories:

Process(es)

cell differentiation

Function(s)

ATP binding