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See other SLC16A2 CNV Assays ›
Gene Symbol
SLC16A2
Assay Reference Genome
Location

Chr.X:74461086 on build GRCh38
Cytoband
Xq13.2
Assay ID Hs05670863_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 6567

Gene Name:

 solute carrier family 16 member 2

Gene Aliases:

 AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT

Location:

 Chr.X:74421493-74533929 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC16A2 NM_006517.4 NP_006508.2
AB085789.1 BAC76827.1
CN342861.1
U05315.1 AAB60374.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv521472 Chr.X:74436580 - 74658266 on Build GRCh38 Gain RLIM SLC16A2

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More Information


Additional Information:

For this assay, SNP(s) [rs112669053] 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

Gene Ontology Categories:

Function(s) Process(es)


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