Assay Details
Target Gene Details
Entrez Gene ID: | 23209 |
Gene Name: | megalencephalic leukoencephalopathy with subcortical cysts 1 |
Gene Aliases: |
LVM, MLC, VL |
Location: |
Chr.22:50059391-50085929 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MLC1 | NM_015166.3 | 12 | 2127 | NP_055981.1 |
| NM_139202.2 | 12 | 1766 | NP_631941.1 | |
| XM_011530678.1 | 11 | 1723 | XP_011528980.1 | |
| XM_017028671.1 | 11 | 1555 | XP_016884160.1 | |
| AF319633.1 | 12 | 1689 | AAK60119.1 | |
| AK124264.1 | ||||
| AK297341.1 | 11 | 1487 | ||
| AK299841.1 | 11 | 1535 | ||
| BC028425.2 | 12 | 1726 | AAH28425.1 | |
| BC070042.1 | 12 | 1724 | AAH70042.1 | |
| D25217.3 | 12 | 1803 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv471222 | Chr.22:50024802 - 50157413 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115770001] 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: |
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Genomic Map