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See other SLC25A14 CNV Assays ›
Gene Symbol
SLC25A14
Assay Reference Genome
Location

Chr.X:130343173 on build GRCh38
Cytoband
Xq26.1
Assay ID Hs05613621_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 9016

Gene Name:

 solute carrier family 25 member 14

Gene Aliases:

 BMCP1, UCP5

Location:

 Chr.X:130339888-130373361 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC25A14 NM_001282195.1 NP_001269124.1
NM_001282196.1 NP_001269125.1
NM_001282197.1 NP_001269126.1
NM_001282198.1 NP_001269127.1
NR_104107.1
XM_005262489.4 XP_005262546.1
XM_011531402.2 XP_011529704.1
XM_011531403.1 XP_011529705.1
XM_017029936.1 XP_016885425.1
XM_017029937.1 XP_016885426.1
XM_017029938.1 XP_016885427.1
XM_017029939.1 XP_016885428.1
XM_017029940.1 XP_016885429.1
XM_017029941.1 XP_016885430.1
AF078544.1 AAD04346.1
AF155809.1 AAG29582.1
AF155810.1 AAG29583.1
AF155811.1 AAG29584.1
AK296155.1
AK297499.1
AK304649.1
AK309433.1
AL520510.3
AY358099.1 AAQ88466.1
BC119666.2
BC119667.1
DB485834.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv528290 Chr.X:129635682 - 130429852 on Build GRCh38 Gain SASH3 SLC25A14 BCORL1 ZDHHC9 XPNPEP2 GPR119 RBMX2 UTP14A APLN ZNF280C ELF4 RAB33A AIFM1

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More Information


Additional Information:

For this assay, SNP(s) [rs144813251] 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:

Gene Ontology Categories:

Function(s) Process(es)


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