Genomic Map
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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: | Within Intron 3 |
| 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: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FNTB | NM_002028.3 | NP_002019.1 | ||
| AK225917.1 | ||||
| AK315714.1 | ||||
| AU122768.1 | ||||
| BC020232.1 | AAH20232.1 | |||
| BX248269.1 | CAD62597.1 | |||
| L00635.1 | AAA35854.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion |
 MIR548H1
FUT8-AS1
SGPP1
MIR4706
MIR4708
MIR625
MTHFD1
FNTB
ZBTB25
LOC100128233
MIR7855
AKAP5
LOC102723809
PPP1R36
GPX2
TEX21P
CHURC1-FNTB
CHURC1
ESR2
GPHN
FUT8
SPTB
RAB15
ZBTB1
MAX
LOC100506321
LINC00238
SYNE2
PLEKHG3
HSPA2
|
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Additional Information:
For this assay, SNP(s) [rs77567418] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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