Hs04397592_cn

• Gene Symbol: MS4A14
• Assay Reference Genome Location: Chr.11:60403866 on build GRCh38
• Cytoband: 11q12.2

Target Gene Details

• Entrez Gene ID: 84689
• Gene Name: membrane spanning 4-domains A14
• Gene Aliases: MS4A16, NYD-SP21
• Location: Chr.11:60396014-60417756 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MS4A14	NM_001079692.2			NP_001073160.1
	NM_001261827.1			NP_001248756.1
	NM_001261828.1			NP_001248757.1
	NM_032597.4			NP_115986.3
	NR_049731.1
	NR_049732.1
	NR_049733.1
	NR_049734.1
	AF367473.2			AAK53409.2
	AK057418.1
	AK314674.1
	AY094610.1			AAM48587.1
	AY094611.1			AAM48588.1
	AY584610.1
	BC107431.1			AAI07432.1
	DB082055.1
	DB450359.2
	DB727789.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2744569	Chr.11:60310239 - 60485227 on Build GRCh38	Deletion	MS4A5 MS4A6E MS4A14 MS4A7 MS4A1

More Information

Additional Information:

For this assay, SNP(s) [rs115464944] 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

Panther Classification:

Molecular Function -

transporter