Genomic Map
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Target Gene Details
Entrez Gene ID: | 51222 |
Gene Name: | zinc finger protein 219 |
Gene Aliases: |
ZFP219 |
Location: |
Chr.14:21090046-21104704 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ZNF219 | NM_001101672.1 | 5 | 2647 | NP_001095142.1 |
| NM_001102454.1 | 5 | 2637 | NP_001095924.1 | |
| NM_016423.2 | 5 | 2781 | NP_057507.2 | |
| XM_005267739.1 | 5 | 2592 | XP_005267796.1 | |
| XM_006720163.2 | 5 | 2528 | XP_006720226.1 | |
| XM_006720164.3 | 5 | 2530 | XP_006720227.1 | |
| XM_011536825.1 | 5 | 2602 | XP_011535127.1 | |
| XM_017021354.1 | 4 | 2597 | XP_016876843.1 | |
| XM_017021355.1 | 5 | 2493 | XP_016876844.1 | |
| AB015427.1 | 5 | 2771 | BAA90526.1 | |
| AK056261.1 | 3 | 1988 | ||
| AK225811.1 | 5 | 2544 | ||
| AK290700.1 | ||||
| BC000694.2 | 4 | 2392 | AAH00694.1 | |
| BC036105.1 | 5 | 2473 | AAH36105.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv123n21 | Chr.14:21072704 - 21106531 on Build GRCh38 | Loss |
 ZNF219
ARHGEF40
TMEM253
|
| nsv826882 | Chr.14:21042862 - 21136042 on Build GRCh38 | Gain |
RNASE8
ZNF219
NDRG2
ARHGEF40
RNASE7
TMEM253
|
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Additional Information:
For this assay, SNP(s) [rs200238223] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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