Hs04024484_cn

• Gene Symbol: CD22
• Assay Reference Genome Location: Chr.19:35330660 on build GRCh38
• Cytoband: 19q13.12

Target Gene Details

• Entrez Gene ID: 933
• Gene Name: CD22 molecule
• Gene Aliases: SIGLEC-2, SIGLEC2
• Location: Chr.19:35329166-35347361 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CD22	NM_001185099.1			NP_001172028.1
	NM_001185100.1			NP_001172029.1
	NM_001185101.1			NP_001172030.1
	NM_001278417.1			NP_001265346.1
	NM_001771.3			NP_001762.2
	AK026467.1			BAB15489.1
	AK225625.1
	AK225694.1
	AK301177.1
	BC109306.1			AAI09307.1
	CF138699.1
	DA931592.1
	DA989528.1
	X59350.1			CAA42006.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833810	Chr.19:35291685 - 35481057 on Build GRCh38	Gain	FFAR2 FFAR1 LINC01531 MIR5196 MAG FFAR3 CD22
esv2758758	Chr.19:35220175 - 35396211 on Build GRCh38	Loss	HAMP FFAR1 FAM187B LSR MIR5196 USF2 MAG FFAR3 CD22
nsv510765	Chr.19:35217323 - 35399766 on Build GRCh38	Deletion	HAMP FFAR1 FAM187B LSR MIR5196 USF2 MAG FFAR3 CD22

More Information

Additional Information:

For this assay, SNP(s) [rs78452397] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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

Gene Ontology Categories:

Process(es)

cell adhesion

Function(s)

protein binding
carbohydrate binding