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 10 - Exon 11 |
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 | ||||
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 | KIAA0895L CENPT ACD LOC105369155 EXOC3L1 FHOD1 LOC107984813 AGRP NUTF2 GFOD2 DDX28 E2F4 ENKD1 PSKH1 THAP11 FAM65A RANBP10 LRRC29 ELMO3 TSNAXIP1 FBXL8 ZDHHC1 LOC100505942 LOC100131303 C16orf86 TRADD DPEP3 DUS2 SLC9A5 ATP6V0D1 PARD6A TMEM208 NOL3 HSF4 LCAT EDC4 TPPP3 DPEP2 KCTD19 CTRL LRRC36 CARMIL2 NRN1L PLEKHG4 SLC12A4 CTCF PSMB10 HSD11B2 MIR328 |
nsv827707 | Chr.16:67148355 - 67289296 on Build GRCh38 | Loss | KIAA0895L C16orf70 TRADD LOC105369155 EXOC3L1 FHOD1 PLEKHG4 SLC9A5 LRRC29 E2F4 ELMO3 TMEM208 FBXL8 NOL3 HSF4 B3GNT9 MIR328 |
nsv952044 | Chr.16:67141198 - 67244397 on Build GRCh38 | Deletion | KIAA0895L C16orf70 TRADD LOC105369155 EXOC3L1 FHOD1 LRRC29 E2F4 ELMO3 TMEM208 FBXL8 NOL3 HSF4 B3GNT9 MIR328 |
nsv1160429 | Chr.16:67161549 - 67220197 on Build GRCh38 | Deletion | KIAA0895L ELMO3 LOC105369155 EXOC3L1 FBXL8 NOL3 HSF4 LRRC29 MIR328 E2F4 |
nsv524363 | Chr.16:67136529 - 68071571 on Build GRCh38 | Loss | KIAA0895L CENPT ACD LOC105369155 EXOC3L1 FHOD1 LOC107984813 AGRP NUTF2 GFOD2 DDX28 E2F4 ENKD1 PSKH1 THAP11 FAM65A RANBP10 LRRC29 ELMO3 TSNAXIP1 FBXL8 ZDHHC1 LOC100505942 LOC100131303 C16orf86 TRADD DPEP3 DUS2 SLC9A5 ATP6V0D1 PARD6A TMEM208 NOL3 HSF4 LCAT B3GNT9 EDC4 TPPP3 DPEP2 KCTD19 CTRL LRRC36 C16orf70 CARMIL2 NRN1L PLEKHG4 SLC12A4 CTCF PSMB10 HSD11B2 MIR328 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |