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 Exon 6 - Intron 6 |
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 Exon 4 - Intron 4 |
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 | ||||
AU122768.1 | ||||
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 | LOC100506321 FNTB CHURC1-FNTB MAX MIR4706 |
esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion | CHURC1 SYNE2 FNTB MIR548H1 SPTB CHURC1-FNTB ESR2 MIR4706 GPX2 LINC00238 RAB15 LOC100506321 TEX21P ZBTB25 LOC102723809 AKAP5 LOC100128233 ZBTB1 SGPP1 PLEKHG3 MAX PPP1R36 GPHN MIR4708 FUT8-AS1 HSPA2 FUT8 MIR625 MIR7855 MTHFD1 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |