Assay Details
Target Gene Details
Entrez Gene ID: | 79750 |
Gene Name: | zinc finger protein 385D |
Gene Aliases: |
ZNF659 |
Location: |
Chr.3:21418419-22372641 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 19 - Exon 20 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZNF385D | NM_024697.2 | NP_078973.1 | ||
XM_017007191.1 | XP_016862680.1 | |||
XM_017007192.1 | XP_016862681.1 | |||
XM_017007193.1 | XP_016862682.1 | |||
XM_017007194.1 | XP_016862683.1 | |||
XM_017007195.1 | XP_016862684.1 | |||
XM_017007196.1 | XP_016862685.1 | |||
XM_017007197.1 | XP_016862686.1 | |||
XM_017007198.1 | XP_016862687.1 | |||
XM_017007199.1 | XP_016862688.1 | |||
XM_017007200.1 | XP_016862689.1 | |||
XM_017007201.1 | XP_016862690.1 | |||
XM_017007202.1 | XP_016862691.1 | |||
AK026072.1 | BAB15350.1 | |||
BC007212.1 | AAH07212.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1006471 | Chr.3:21344135 - 21555463 on Build GRCh38 | Gain |
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nsv238000 | Chr.3:21416042 - 21424317 on Build GRCh38 | Deletion |
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nsv834630 | Chr.3:21270127 - 21449835 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs76423389] 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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Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)