Hs01564172_cn

• Gene Symbol: SLFN5
• Assay Reference Genome Location: Chr.17:35259154 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 Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLFN5	NM_144975.3	2	581	NP_659412.3
	XM_005257934.3	2	622	XP_005257991.1
	AK054668.1	2	576	BAB70788.1
	AK303299.1	2	576
	AK303632.1	2	578
	BC021238.1	2	559	AAH21238.1
	BC125200.1	1	517
	BC125201.1	1	517
	BP281007.1
	BX647942.1	2	578

Target Copy Number Variation Details

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

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

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

cell differentiation

Function(s)

ATP binding