Assay Details
Target Gene Details
Entrez Gene ID: | 3299 |
Gene Name: | heat shock transcription factor 4 |
Gene Aliases: |
CTM, CTRCT5 |
Location: |
Chr.16:67163385-67169945 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 6 - Intron 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
HSF4 | NM_001040667.2 | NP_001035757.1 | ||
NM_001538.3 | NP_001529.2 | |||
AB029348.1 | BAA84582.1 | |||
AK225152.1 | ||||
AK293631.1 | ||||
AK296210.1 | ||||
D87673.1 | BAA13433.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv522852 | Chr.16:67153308 - 68071571 on Build GRCh38 | Gain | GFOD2 PARD6A LOC107984813 C16orf86 KIAA0895L CTRL LRRC36 DDX28 LOC100505942 PSMB10 TPPP3 TMEM208 THAP11 ENKD1 LOC105369155 PSKH1 ACD CENPT DPEP2 NUTF2 SLC9A5 FHOD1 TRADD ZDHHC1 HSD11B2 PLEKHG4 TSNAXIP1 NOL3 FAM65A RANBP10 NRN1L CTCF LOC100131303 ELMO3 DUS2 ATP6V0D1 LRRC29 FBXL8 KCTD19 HSF4 CARMIL2 MIR328 EDC4 LCAT SLC12A4 AGRP DPEP3 E2F4 EXOC3L1 |
nsv827707 | Chr.16:67148355 - 67289296 on Build GRCh38 | Loss | MIR328 LOC105369155 B3GNT9 KIAA0895L ELMO3 SLC9A5 FHOD1 TRADD C16orf70 LRRC29 FBXL8 PLEKHG4 TMEM208 E2F4 EXOC3L1 HSF4 NOL3 |
nsv952044 | Chr.16:67141198 - 67244397 on Build GRCh38 | Deletion | MIR328 LOC105369155 B3GNT9 KIAA0895L ELMO3 FHOD1 TRADD C16orf70 LRRC29 FBXL8 TMEM208 E2F4 EXOC3L1 HSF4 NOL3 |
nsv1160429 | Chr.16:67161549 - 67220197 on Build GRCh38 | Deletion | MIR328 LOC105369155 LRRC29 FBXL8 KIAA0895L ELMO3 E2F4 EXOC3L1 HSF4 NOL3 |
nsv524363 | Chr.16:67136529 - 68071571 on Build GRCh38 | Loss | GFOD2 PARD6A LOC107984813 C16orf86 B3GNT9 KIAA0895L CTRL LRRC36 DDX28 LOC100505942 C16orf70 PSMB10 TPPP3 TMEM208 THAP11 ENKD1 LOC105369155 PSKH1 ACD CENPT DPEP2 NUTF2 SLC9A5 FHOD1 TRADD ZDHHC1 HSD11B2 PLEKHG4 TSNAXIP1 NOL3 FAM65A RANBP10 NRN1L CTCF LOC100131303 ELMO3 DUS2 ATP6V0D1 LRRC29 FBXL8 KCTD19 HSF4 CARMIL2 MIR328 EDC4 LCAT SLC12A4 AGRP DPEP3 E2F4 EXOC3L1 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |