Assay Details
Target Gene Details
Entrez Gene ID: | 55628 |
Gene Name: | zinc finger protein 407 |
Gene Aliases: |
- |
Location: |
Chr.18:74597735-75065672 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZNF407 | XM_005266726.4 | XP_005266783.1 | ||
XM_006722500.3 | XP_006722563.1 | |||
XM_011526068.2 | XP_011524370.1 | |||
XM_011526069.2 | XP_011524371.1 | |||
XM_011526070.1 | XP_011524372.1 | |||
XM_017025838.1 | XP_016881327.1 | |||
AK056288.1 | BAB71139.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1057441 | Chr.18:74344906 - 74669985 on Build GRCh38 | Gain | C18orf63 LINC00909 ZNF407 CNDP1 LOC101927606 CNDP2 FAM69C |
nsv577656 | Chr.18:74534683 - 75005167 on Build GRCh38 | Gain | LINC00909 ZNF407 CNDP1 |
esv3643124 | Chr.18:74623637 - 74695240 on Build GRCh38 | Gain | ZNF407 |
More Information
Additional Information:
For this assay, SNP(s) [rs139171681] 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 |