Assay Details
Target Gene Details
Entrez Gene ID: | 9328 |
Gene Name: | general transcription factor IIIC subunit 5 |
Gene Aliases: |
TFIIIC63, TFIIICepsilon, TFiiiC2-63 |
Location: |
Chr.9:133030675-133058503 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GTF3C5 | NM_001122823.1 | 1 | 132 | NP_001116295.1 |
NM_001286709.1 | 1 | 132 | NP_001273638.1 | |
NM_012087.3 | 1 | 132 | NP_036219.2 | |
XM_005272234.3 | 1 | 127 | XP_005272291.1 | |
XM_011519201.1 | 1 | 114 | XP_011517503.1 | |
XM_017015315.1 | 1 | 114 | XP_016870804.1 | |
XM_017015316.1 | 1 | 114 | XP_016870805.1 | |
AF133124.1 | 1 | 87 | AAD41476.1 | |
AK055092.1 | 1 | 94 | ||
AK225761.1 | 1 | 99 | ||
AK311481.1 | 1 | 97 | ||
BC011355.1 | 1 | 76 | AAH11355.1 | |
BC017337.2 | 1 | 55 | AAH17337.1 | |
DB194811.1 | 1 | 132 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2739138 | Chr.9:132727483 - 135521553 on Build GRCh38 | Deletion | LOC401557 SNORD36C COL5A1-AS1 MIR3689E FCN2 WDR5 C9orf116 OBP2B PPP1R26 LOC100996574 GFI1B COL5A1 SNORD36A TSC1 MIR3689D1 GTF3C5 FAM163B LOC105376306 CACFD1 MIR548AW MRPS2 MED22 RNU6ATAC DBH-AS1 ADAMTSL2 ABO SURF6 SNORD24 VAV2 MIR3689D2 STKLD1 C9orf62 ADAMTS13 LOC101448202 LOC100130548 SNORD141A MIR3689F DBH LINC00094 MIR3689C SURF4 CEL OLFM1 MIR3689B SPACA9 RXRA PPP1R26-AS1 REXO4 MIR6877 SNORD36B GBGT1 SURF2 RALGDS LOC101928193 MIR4669 RPL7A SLC2A6 LOC101928525 TMEM8C SARDH CELP LCN1 FCN1 MIR3689A SURF1 BRD3 AK8 |
nsv615596 | Chr.9:133030314 - 133080285 on Build GRCh38 | Loss | LOC100996574 MIR6877 CEL GTF3C5 LOC105376306 |
nsv831744 | Chr.9:132980050 - 133174043 on Build GRCh38 | Gain+Loss | LOC100996574 MIR6877 GFI1B GBGT1 CELP CEL SNORD141A GTF3C5 RALGDS LOC105376306 |
nsv508564 | Chr.9:133013830 - 133073076 on Build GRCh38 | Deletion | LOC100996574 MIR6877 CEL SNORD141A GTF3C5 LOC105376306 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |