accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other TLDC1 CNV Assays ›
Gene Symbol
TLDC1
Assay Reference Genome
Location

Chr.16:84479208 on build GRCh38
Cytoband
16q24.1
Assay ID Hs01802836_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 57707

Gene Name:

 TBC/LysM-associated domain containing 1

Gene Aliases:

 KIAA1609

Location:

 Chr.16:84476355-84504752 on Build GRCh38

Assay Gene Location:

 Within Exon 12
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TLDC1 NM_020947.3 8 2183 NP_065998.3
XM_005256074.3 8 2253 XP_005256131.1
XM_005256075.2 9 2381 XP_005256132.1
XM_006721240.2 9 2336 XP_006721303.1
XM_011523248.2 10 2480 XP_011521550.1
XM_017023510.1 10 2500 XP_016878999.1
XM_017023511.1 8 2255 XP_016879000.1
XM_017023512.1 9 2423 XP_016879001.1
AA115393.1 1 259
AK297241.1 5 1241
AL137316.1 3 1052 CAB70693.1
BC060844.1 9 2113 AAH60844.1
CB160601.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1065249 Chr.16:84435765 - 84556540 on Build GRCh38 Gain TLDC1 LOC105371374 ATP2C2
nsv1061004 Chr.16:84405376 - 84561748 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
dgv169n21 Chr.16:84346305 - 84480735 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
esv3892928 Chr.16:84339110 - 84524557 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
nsv573425 Chr.16:84298994 - 84575953 on Build GRCh38 Loss WFDC1 TLDC1 LOC105371374 COTL1 ATP2C2
nsv1064308 Chr.16:84461124 - 84592674 on Build GRCh38 Loss TLDC1 LOC105371374 COTL1 ATP2C2
esv3639429 Chr.16:84472177 - 84518552 on Build GRCh38 Gain TLDC1
dgv3057n100 Chr.16:84378422 - 84500091 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
nsv483044 Chr.16:84166395 - 87066394 on Build GRCh38 Gain TAF1C LOC146513 FLJ30679 FENDRR GSE1 LOC102724344 KCNG4 KIAA0513 ZDHHC7 FOXC2-AS1 IRF8 MTHFSD USP10 FOXC2 TLDC1 LINC00917 LOC101928614 MIR6774 MIR1910 LINC01081 CRISPLD2 LOC105371374 LINC01082 DNAAF1 ADAD2 COX4I1 LOC400548 KLHL36 FAM92B LOC101928557 MIR5093 FOXL1 ATP2C2 LINC00311 WFDC1 GINS2 FOXF1 LOC101928474 COTL1 LOC440390 LOC105376777 C16orf74 EMC8
nsv573454 Chr.16:84468700 - 84512067 on Build GRCh38 Loss TLDC1
nsv1059640 Chr.16:84338790 - 84543759 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
esv2714828 Chr.16:84478872 - 84480027 on Build GRCh38 Deletion TLDC1
dgv5262n54 Chr.16:84381903 - 84583279 on Build GRCh38 Loss TLDC1 LOC105371374 COTL1 ATP2C2
nsv573430 Chr.16:84387654 - 84501190 on Build GRCh38 Loss TLDC1 LOC105371374 ATP2C2
dgv549e214 Chr.16:84434443 - 84555604 on Build GRCh38 Gain TLDC1 LOC105371374 ATP2C2

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs142235616] 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

Gene Ontology Categories:

Process(es)


Back To Top

Related Products