Assay Details
Target Gene Details
Entrez Gene ID: | 6945 |
Gene Name: | MLX, MAX dimerization protein |
Gene Aliases: |
MAD7, MXD7, TCFL4, bHLHd13 |
Location: |
Chr.17:42567060-42573203 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MLX | NM_170607.2 | 8 | 1380 | NP_733752.1 |
NM_198204.1 | 8 | 1218 | NP_937847.1 | |
NM_198205.1 | 7 | 1128 | NP_937848.1 | |
XM_017024991.1 | 7 | 1267 | XP_016880480.1 | |
AF203978.1 | 8 | 1168 | AAF14638.1 | |
AF213666.1 | 7 | 1116 | AAG40145.1 | |
AF213667.1 | 8 | 1206 | AAG40146.1 | |
AF213668.1 | 8 | 1368 | AAG40147.1 | |
AK000150.1 | 8 | 1177 | BAA90977.1 | |
AK303221.1 | 8 | 1101 | ||
BC010689.2 | 8 | 1203 | AAH10689.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1064012 | Chr.17:42427786 - 42606703 on Build GRCh38 | Gain | MIR5010 NAGLU PSMC3IP HSD17B1 MIR548AT COASY FAM134C MLX ATP6V0A1 |
More Information
Additional Information:
For this assay, SNP(s) [rs556813574] 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 Exonic DGV Variation |