Genomic Map
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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 18 - Exon 18 |
| 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 |
 ZNF385D
VENTXP7
ZNF385D-AS1
|
| nsv834630 | Chr.3:21270127 - 21449835 on Build GRCh38 | Loss |
ZNF385D
VENTXP7
|
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Additional Information:
For this assay, SNP(s) [rs73820942] 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
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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