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: | Overlaps Intron 12 - Exon 12 |
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 | COLEC12 TYMS TYMSOS ENOSF1 CLUL1 YES1 CETN1 LOC105376854 |
dgv5810n54 | Chr.18:351004 - 2238246 on Build GRCh38 | Gain | LINC00470 COLEC12 TYMS TYMSOS ENOSF1 LOC388456 CLUL1 YES1 CETN1 ADCYAP1 LOC105376854 |
nsv576242 | Chr.18:567127 - 841320 on Build GRCh38 | Gain | TYMS TYMSOS ENOSF1 CLUL1 YES1 CETN1 |
esv3641497 | Chr.18:551569 - 745897 on Build GRCh38 | Gain | TYMS TYMSOS ENOSF1 CLUL1 YES1 CETN1 |
nsv528169 | Chr.18:551688 - 2240220 on Build GRCh38 | Loss | LINC00470 TYMS TYMSOS ENOSF1 LOC388456 CLUL1 YES1 CETN1 ADCYAP1 |
nsv1060188 | Chr.18:575087 - 863351 on Build GRCh38 | Gain | TYMS TYMSOS ENOSF1 CLUL1 YES1 CETN1 |
esv2761984 | Chr.18:724222 - 855263 on Build GRCh38 | Loss | YES1 |
esv3893055 | Chr.18:415105 - 743226 on Build GRCh38 | Gain | COLEC12 TYMS TYMSOS ENOSF1 CLUL1 YES1 CETN1 LOC105376854 |
nsv482935 | Chr.18:10001 - 2900002 on Build GRCh38 | Loss | LINC00470 CBX3P2 TYMSOS ENOSF1 LOC388456 NDC80 LOC105376854 SMCHD1 METTL4 COLEC12 TYMS MIR8078 ROCK1P1 EMILIN2 LOC101926997 CLUL1 THOC1 YES1 CETN1 ADCYAP1 USP14 |
nsv576228 | Chr.18:69836 - 1506323 on Build GRCh38 | Loss | LINC00470 TYMSOS ENOSF1 LOC388456 LOC105376854 COLEC12 TYMS MIR8078 ROCK1P1 CLUL1 THOC1 YES1 CETN1 ADCYAP1 USP14 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |