Assay Details
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 | MAX MIR4706 LOC100506321 CHURC1-FNTB FNTB |
esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion | MAX MIR548H1 PPP1R36 LOC100128233 LOC102723809 MTHFD1 GPX2 LOC100506321 CHURC1-FNTB SYNE2 CHURC1 ZBTB1 AKAP5 MIR4708 FUT8-AS1 FUT8 TEX21P HSPA2 SGPP1 ESR2 PLEKHG3 FNTB MIR7855 GPHN MIR4706 LINC00238 RAB15 SPTB MIR625 ZBTB25 |
More Information
Additional Information:
For this assay, SNP(s) [rs115853099] 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 |