Assay Details
Target Gene Details
Entrez Gene ID: | 7264 |
Gene Name: | tissue specific transplantation antigen P35B |
Gene Aliases: |
FX, P35B, SDR4E1 |
Location: |
Chr.8:143612618-143618043 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TSTA3 | NM_001317783.1 | NP_001304712.1 | ||
NM_003313.3 | NP_003304.1 | |||
XM_005251051.3 | XP_005251108.2 | |||
XM_011517269.1 | XP_011515571.1 | |||
AK096752.1 | ||||
AK303125.1 | ||||
AK313560.1 | ||||
BC001941.1 | AAH01941.1 | |||
BC093061.1 | AAH93061.1 | |||
BG709420.1 | ||||
U58766.1 | AAC50786.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv12427n54 | Chr.8:143615483 - 143632493 on Build GRCh38 | Loss | TSTA3 |
nsv950013 | Chr.8:143465031 - 143616230 on Build GRCh38 | Deletion | MROH6 TSTA3 TIGD5 PYCRL NAPRT GSDMD ZC3H3 EEF1D |
nsv612777 | Chr.8:143538914 - 143632493 on Build GRCh38 | Gain | MROH6 TSTA3 TIGD5 PYCRL NAPRT GSDMD ZC3H3 EEF1D |
nsv1161810 | Chr.8:143542268 - 143622987 on Build GRCh38 | Deletion | MROH6 TSTA3 TIGD5 PYCRL NAPRT GSDMD ZC3H3 EEF1D |
esv3584899 | Chr.8:143611680 - 143636819 on Build GRCh38 | Loss | TSTA3 ZNF623 |
nsv42 | Chr.8:143610600 - 143635500 on Build GRCh38 | Deletion | TSTA3 |
nsv6439 | Chr.8:143606519 - 143651282 on Build GRCh38 | Deletion | TSTA3 PYCRL ZNF623 |
nsv612793 | Chr.8:143552167 - 143630578 on Build GRCh38 | Loss | MROH6 TSTA3 TIGD5 PYCRL NAPRT GSDMD EEF1D |
dgv7336n100 | Chr.8:143510004 - 143616975 on Build GRCh38 | Gain | MROH6 TSTA3 TIGD5 PYCRL NAPRT GSDMD ZC3H3 EEF1D |
dgv271n111 | Chr.8:143601764 - 143642893 on Build GRCh38 | Deletion | TSTA3 PYCRL ZNF623 |
nsv831488 | Chr.8:143590454 - 143684444 on Build GRCh38 | Loss | TSTA3 TIGD5 PYCRL EEF1D ZNF623 |
nsv466004 | Chr.8:143581491 - 143640022 on Build GRCh38 | Loss | TSTA3 TIGD5 PYCRL EEF1D ZNF623 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |