Genomic Map
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Target Gene Details
Entrez Gene ID: | 90075 |
Gene Name: | zinc finger protein 30 |
Gene Aliases: |
KOX28 |
Location: |
Chr.19:34923795-34945172 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 7 - Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ZNF30 | NM_001099437.1 | NP_001092907.1 | ||
| NM_001099438.1 | NP_001092908.1 | |||
| NM_194325.2 | NP_919306.2 | |||
| NR_024018.1 | ||||
| XM_011527443.2 | XP_011525745.1 | |||
| XM_011527444.1 | XP_011525746.1 | |||
| XM_017027423.1 | XP_016882912.1 | |||
| XM_017027424.1 | XP_016882913.1 | |||
| XM_017027425.1 | XP_016882914.1 | |||
| XM_017027426.1 | XP_016882915.1 | |||
| XM_017027427.1 | XP_016882916.1 | |||
| XM_017027428.1 | XP_016882917.1 | |||
| XM_017027429.1 | XP_016882918.1 | |||
| AK290435.1 | ||||
| AK295515.1 | ||||
| BC142996.1 | ||||
| BX640666.1 | CAE45802.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2760536 | Chr.19:34939482 - 34994365 on Build GRCh38 | Gain |
 ZNF30
ZNF792
|
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Additional Information:
For this assay, SNP(s) [rs76732057] 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
|
Panther Classification:
Gene Ontology Categories:
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