Hs02142705_cn

• Gene Symbol: SNX22
• Assay Reference Genome Location: Chr.15:64153667 on build GRCh38
• Cytoband: 15q22.31

Target Gene Details

• Entrez Gene ID: 79856
• Gene Name: sorting nexin 22
• Gene Aliases: -
• Location: Chr.15:64151698-64157481 on Build GRCh38
• Assay Gene Location: Overlaps Intron 4 - Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SNX22	NM_024798.2			NP_079074.2
	NR_073534.1
	XM_005254677.3			XP_005254734.1
	XM_017022581.1			XP_016878070.1
	AK024014.1			BAB14776.1
	AK126655.1			BAC86630.1
	AL832838.1
	AY044653.1			AAK98767.1
	BC019655.1			AAH19655.1
	BC030225.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833036	Chr.15:64072492 - 64215189 on Build GRCh38	Loss	SNX1 FAM96A CSNK1G1 SNX22 PPIB
nsv827360	Chr.15:64152078 - 64160104 on Build GRCh38	Loss	SNX22 PPIB

More Information

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

Panther Classification:

Molecular Function -

scaffold/adaptor protein

Gene Ontology Categories:

Process(es)

protein transport

Function(s)

phosphatidylinositol binding