Assay Details
Target Gene Details
Entrez Gene ID: | 340156 |
Gene Name: | myosin light chain kinase family member 4 |
Gene Aliases: |
SgK085 |
Location: |
Chr.6:2663629-2770330 on Build GRCh38 |
Assay Gene Location: | Within Intron 16 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MYLK4 | NM_001012418.3 | NP_001012418.2 | ||
XM_005249078.3 | XP_005249135.2 | |||
XM_005249079.2 | XP_005249136.1 | |||
XM_006715082.3 | XP_006715145.1 | |||
XM_011514567.2 | XP_011512869.1 | |||
XM_017010819.1 | XP_016866308.1 | |||
AK122581.1 | BAC56922.1 | |||
AK127360.1 | ||||
BC132831.1 | ||||
BC132833.1 | ||||
BX647582.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3607900 | Chr.6:2093592 - 2775672 on Build GRCh38 | Gain | LINC01600 GMDS WRNIP1 MYLK4 GMDS-AS1 |
esv3607912 | Chr.6:2623291 - 2776818 on Build GRCh38 | Gain | LINC01600 WRNIP1 MYLK4 |
More Information
Additional Information:
For this assay, SNP(s) [rs146924438] 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 |