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See other TACC2 CNV Assays ›
Gene Symbol
TACC2
Assay Reference Genome
Location

Chr.10:122013355 on build GRCh38
Cytoband
10q26.13
Assay ID Hs05113794_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 10579

Gene Name:

 transforming acidic coiled-coil containing protein 2

Gene Aliases:

 AZU-1, ECTACC

Location:

 Chr.10:121989174-122254545 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TACC2 NM_001291876.1 NP_001278805.1
NM_001291877.1 NP_001278806.1
NM_206861.2 NP_996743.1
NM_206862.3 NP_996744.3
XM_005269388.1 XP_005269445.1
XM_005269390.1 XP_005269447.1
XM_005269391.1 XP_005269448.1
XM_005269392.1 XP_005269449.1
XM_005269393.1 XP_005269450.1
XM_005269394.1 XP_005269451.1
XM_005269395.1 XP_005269452.1
XM_005269396.1 XP_005269453.1
XM_005269397.1 XP_005269454.1
XM_005269399.1 XP_005269456.1
XM_006717548.1 XP_006717611.1
XM_006717552.1 XP_006717615.1
XM_006717553.1 XP_006717616.1
XM_006717554.1 XP_006717617.1
XM_011539126.1 XP_011537428.1
XM_011539128.1 XP_011537430.1
XM_011539129.1 XP_011537431.1
XM_011539130.1 XP_011537432.1
XM_017015484.1 XP_016870973.1
XM_017015485.1 XP_016870974.1
XM_017015486.1 XP_016870975.1
XM_017015487.1 XP_016870976.1
XM_017015488.1 XP_016870977.1
XM_017015489.1 XP_016870978.1
XM_017015490.1 XP_016870979.1
AF528098.1 AAO62629.1
AF528099.1 AAO62630.1
AK094848.1
AL833304.1
BC144599.1
BC144600.1
BC150627.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1051882 Chr.10:121995657 - 122018988 on Build GRCh38 Loss TACC2
nsv1045815 Chr.10:121986932 - 122086108 on Build GRCh38 Loss TACC2

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More Information


Additional Information:

For this assay, SNP(s) [rs75906629] 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:

Function(s) Process(es)


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