Assay Details
Target Gene Details
Entrez Gene ID: | 7525 |
Gene Name: | YES proto-oncogene 1, Src family tyrosine kinase |
Gene Aliases: |
HsT441, P61-YES, Yes, c-yes |
Location: |
Chr.18:721592-812326 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
YES1 | NM_005433.3 | NP_005424.1 | ||
XM_005258139.3 | XP_005258196.1 | |||
XM_017025960.1 | XP_016881449.1 | |||
AK314063.1 | ||||
BC048960.1 | AAH48960.1 | |||
M15990.1 | AAA35735.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv576236 | Chr.18:319176 - 794272 on Build GRCh38 | Gain | YES1 TYMS LOC105376854 CETN1 ENOSF1 COLEC12 CLUL1 TYMSOS |
dgv5810n54 | Chr.18:351004 - 2238246 on Build GRCh38 | Gain | YES1 TYMS LOC105376854 CETN1 LOC388456 ADCYAP1 ENOSF1 COLEC12 LINC00470 CLUL1 TYMSOS |
nsv576242 | Chr.18:567127 - 841320 on Build GRCh38 | Gain | YES1 TYMS CETN1 ENOSF1 CLUL1 TYMSOS |
nsv528169 | Chr.18:551688 - 2240220 on Build GRCh38 | Loss | YES1 TYMS CETN1 LOC388456 ADCYAP1 ENOSF1 LINC00470 CLUL1 TYMSOS |
nsv1060188 | Chr.18:575087 - 863351 on Build GRCh38 | Gain | YES1 TYMS CETN1 ENOSF1 CLUL1 TYMSOS |
nsv1057808 | Chr.18:766118 - 803577 on Build GRCh38 | Loss | YES1 |
esv2761984 | Chr.18:724222 - 855263 on Build GRCh38 | Loss | YES1 |
nsv482935 | Chr.18:10001 - 2900002 on Build GRCh38 | Loss | YES1 LOC105376854 CETN1 CBX3P2 ADCYAP1 ENOSF1 THOC1 USP14 COLEC12 LINC00470 EMILIN2 METTL4 TYMSOS TYMS LOC388456 NDC80 LOC101926997 ROCK1P1 MIR8078 CLUL1 SMCHD1 |
nsv576228 | Chr.18:69836 - 1506323 on Build GRCh38 | Loss | YES1 LOC105376854 CETN1 ADCYAP1 ENOSF1 THOC1 USP14 COLEC12 LINC00470 TYMSOS TYMS LOC388456 ROCK1P1 MIR8078 CLUL1 |
More Information
Additional Information:
For this assay, SNP(s) [rs79946736] 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 |