Assay Details
Target Gene Details
Entrez Gene ID: | 100529261 |
Gene Name: | CHURC1-FNTB readthrough |
Gene Aliases: |
- |
Location: |
Chr.14:64914361-65062655 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 8 - Exon 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CHURC1-FNTB | NM_001202558.1 | NP_001189487.1 | ||
NM_001202559.1 | NP_001189488.1 | |||
AK296850.1 | ||||
AK303739.1 |
Target Gene Details
Entrez Gene ID: | 2342 |
Gene Name: | farnesyltransferase, CAAX box, beta |
Gene Aliases: |
FPTB |
Location: |
Chr.14:64986789-65062652 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 6 - Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FNTB | NM_002028.3 | NP_002019.1 | ||
AK093298.1 | ||||
AK225917.1 | ||||
AK295972.1 | ||||
AK315714.1 | ||||
BC020232.1 | AAH20232.1 | |||
BX248269.1 | CAD62597.1 | |||
L00635.1 | AAA35854.1 | |||
L10414.1 | AAA86286.1 |
Target Gene Details
Entrez Gene ID: | 4149 |
Gene Name: | MYC associated factor X |
Gene Aliases: |
bHLHd4 |
Location: |
Chr.14:65006101-65102695 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MAX | NM_001271069.1 | NP_001257998.1 | ||
NM_197957.3 | NP_932061.1 | |||
AI652319.1 | ||||
AI655674.1 | ||||
AI917842.1 | ||||
DB482510.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832816 | Chr.14:65006526 - 65177927 on Build GRCh38 | Gain | CHURC1-FNTB MAX FNTB MIR4706 LOC100506321 |
esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion | TEX21P RAB15 FNTB MIR4706 LOC100506321 HSPA2 LOC100128233 MIR625 LINC00238 CHURC1-FNTB SGPP1 FUT8 MIR7855 SPTB PPP1R36 GPX2 CHURC1 ZBTB25 AKAP5 ZBTB1 GPHN SYNE2 MTHFD1 MAX ESR2 MIR4708 MIR548H1 FUT8-AS1 LOC102723809 PLEKHG3 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |