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 8 - Exon 9 |
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 | DPEP3 EXOC3L1 HSD11B2 PSKH1 TRADD NOL3 FAM65A ZDHHC1 LOC107984813 SLC12A4 TMEM208 ELMO3 THAP11 PSMB10 CENPT AGRP LOC100505942 ACD MIR328 CARMIL2 DPEP2 PLEKHG4 ENKD1 C16orf86 KCTD19 DDX28 CTRL RANBP10 FHOD1 GFOD2 DUS2 FBXL8 LRRC36 LCAT SLC9A5 NRN1L HSF4 E2F4 LOC105369155 TPPP3 ATP6V0D1 EDC4 LRRC29 PARD6A TSNAXIP1 LOC100131303 CTCF KIAA0895L NUTF2 |
nsv827707 | Chr.16:67148355 - 67289296 on Build GRCh38 | Loss | FHOD1 C16orf70 TMEM208 ELMO3 FBXL8 EXOC3L1 LRRC29 MIR328 SLC9A5 PLEKHG4 TRADD KIAA0895L NOL3 HSF4 E2F4 LOC105369155 B3GNT9 |
nsv952044 | Chr.16:67141198 - 67244397 on Build GRCh38 | Deletion | FHOD1 C16orf70 TMEM208 ELMO3 FBXL8 EXOC3L1 LRRC29 MIR328 TRADD KIAA0895L NOL3 HSF4 E2F4 LOC105369155 B3GNT9 |
nsv1160429 | Chr.16:67161549 - 67220197 on Build GRCh38 | Deletion | MIR328 KIAA0895L ELMO3 NOL3 FBXL8 EXOC3L1 LRRC29 HSF4 E2F4 LOC105369155 |
nsv524363 | Chr.16:67136529 - 68071571 on Build GRCh38 | Loss | C16orf70 DPEP3 EXOC3L1 HSD11B2 PSKH1 TRADD NOL3 FAM65A ZDHHC1 LOC107984813 SLC12A4 TMEM208 ELMO3 THAP11 PSMB10 CENPT AGRP LOC100505942 ACD MIR328 CARMIL2 DPEP2 PLEKHG4 ENKD1 C16orf86 KCTD19 DDX28 CTRL RANBP10 FHOD1 GFOD2 DUS2 FBXL8 LRRC36 LCAT SLC9A5 NRN1L HSF4 E2F4 LOC105369155 TPPP3 ATP6V0D1 EDC4 LRRC29 PARD6A TSNAXIP1 LOC100131303 CTCF KIAA0895L NUTF2 B3GNT9 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |