Assay Details
Target Gene Details
Entrez Gene ID: | 9097 |
Gene Name: | ubiquitin specific peptidase 14 |
Gene Aliases: |
TGT |
Location: |
Chr.18:158483-213739 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
USP14 | NM_001037334.1 | NP_001032411.1 | ||
NM_005151.3 | NP_005142.1 | |||
AK095516.1 | ||||
AK297605.1 | ||||
AK315438.1 | ||||
BC003556.1 | AAH03556.1 | |||
BG717018.1 | ||||
BT007183.1 | AAP35847.1 | |||
CR976282.1 | ||||
U30888.1 | AAB60365.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv576227 | Chr.18:52933 - 322183 on Build GRCh38 | Gain | USP14 COLEC12 ROCK1P1 MIR8078 THOC1 |
esv3641475 | Chr.18:153985 - 282924 on Build GRCh38 | Gain | USP14 THOC1 |
nsv1064150 | Chr.18:99036 - 321710 on Build GRCh38 | Gain | USP14 COLEC12 ROCK1P1 MIR8078 THOC1 |
dgv3301n100 | Chr.18:11543 - 326679 on Build GRCh38 | Gain | USP14 COLEC12 ROCK1P1 MIR8078 THOC1 |
nsv482935 | Chr.18:10001 - 2900002 on Build GRCh38 | Loss | CBX3P2 TYMSOS METTL4 ENOSF1 COLEC12 YES1 CETN1 LOC105376854 ROCK1P1 LOC388456 MIR8078 THOC1 LINC00470 USP14 EMILIN2 ADCYAP1 CLUL1 LOC101926997 SMCHD1 NDC80 TYMS |
dgv3302n100 | Chr.18:136228 - 249310 on Build GRCh38 | Gain | USP14 THOC1 |
esv3641473 | Chr.18:128077 - 323706 on Build GRCh38 | Gain | USP14 COLEC12 THOC1 |
nsv576228 | Chr.18:69836 - 1506323 on Build GRCh38 | Loss | TYMSOS ENOSF1 COLEC12 YES1 CETN1 LOC105376854 ROCK1P1 LOC388456 MIR8078 THOC1 LINC00470 USP14 ADCYAP1 CLUL1 TYMS |
esv3573886 | Chr.18:136227 - 218394 on Build GRCh38 | Gain | USP14 THOC1 |
More Information
Additional Information:
For this assay, SNP(s) [rs114034581] 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 |