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See other TBC1D5 CNV Assays ›
Gene Symbol
TBC1D5
Assay Reference Genome
Location

Chr.3:17157945 on build GRCh38
Cytoband
3p24.3
Assay ID Hs06646790_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 9779

Gene Name:

 TBC1 domain family member 5

Gene Aliases:

 -

Location:

 Chr.3:17157162-17742739 on Build GRCh38

Assay Gene Location:

 Within Exon 35
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TBC1D5 NM_001134381.1 24 5736 NP_001127853.1
NM_014744.2 22 7071 NP_055559.1
XM_005265611.1 23 5707 XP_005265668.1
XM_005265612.1 22 5642 XP_005265669.1
XM_005265614.1 22 5641 XP_005265671.1
XM_005265615.1 22 5637 XP_005265672.1
XM_005265616.4 21 5566 XP_005265673.1
XM_006713430.1 23 5757 XP_006713493.1
XM_011534281.1 25 6018 XP_011532583.1
XM_011534283.2 24 5796 XP_011532585.1
XM_011534284.2 24 5841 XP_011532586.1
XM_011534286.1 23 5773 XP_011532588.1
XM_011534287.1 23 5755 XP_011532589.1
XM_017007552.1 26 6119 XP_016863041.1
XM_017007553.1 26 6149 XP_016863042.1
XM_017007554.1 31 6762 XP_016863043.1
XM_017007555.1 25 6001 XP_016863044.1
XM_017007556.1 24 5981 XP_016863045.1
XM_017007557.1 21 5535 XP_016863046.1
XM_017007558.1 21 5565 XP_016863047.1
XM_017007559.1 23 5915 XP_016863048.1
XM_017007560.1 23 5745 XP_016863049.1
XM_017007561.1 21 5576 XP_016863050.1
XM_017007562.1 23 5755 XP_016863051.1
XM_017007563.1 20 5495 XP_016863052.1
XM_017007564.1 21 5571 XP_016863053.1
XM_017007565.1 22 5869 XP_016863054.1
XM_017007566.1 22 5658 XP_016863055.1
XM_017007567.1 20 5499 XP_016863056.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1008636 Chr.3:17131923 - 17166775 on Build GRCh38 Gain TBC1D5

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More Information


Additional Information:

For this assay, SNP(s) [rs112962032] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

GTPase-activating protein

Gene Ontology Categories:

Function(s) Process(es)


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