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- Gene Symbol
- DUSP18
- Assay Reference Genome
Location
Chr.22:30667657 on build GRCh38- Cytoband
Genomic Map
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Target Gene Details
Entrez Gene ID: | 150290 |
Gene Name: | dual specificity phosphatase 18 |
Gene Aliases: |
DSP18, DUSP20, LMWDSP20 |
Location: |
Chr.22:30652051-30667875 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DUSP18 | NM_001304794.2 | 1 | 219 | NP_001291723.1 |
| NM_001304795.2 | 1 | 219 | NP_001291724.1 | |
| NM_001304796.2 | 1 | 219 | NP_001291725.1 | |
| NM_152511.5 | 1 | 219 | NP_689724.3 | |
| XM_005261368.6 | 1 | 219 | XP_005261425.1 | |
| XM_011529921.4 | 1 | 219 | XP_011528223.1 | |
| XM_017028627.3 | 1 | 219 | XP_016884116.1 | |
| XM_017028628.2 | 1 | 219 | XP_016884117.1 | |
| XM_047441158.1 | 1 | 219 | XP_047297114.1 | |
| XM_047441159.1 | 1 | 219 | XP_047297115.1 | |
| AF461689.1 | 1 | 229 | AAN77931.1 | |
| AK056074.1 | 1 | 229 | BAG51616.1 | |
| BC030987.1 | 1 | 187 | AAH30987.1 | |
| BM550612.1 | 1 | 213 | ||
| DA378760.1 | 1 | 234 |
Target Gene Details
Entrez Gene ID: | 339665 |
Gene Name: | solute carrier family 35 member E4 |
Gene Aliases: |
- |
Location: |
Chr.22:30635781-30669019 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC35E4 | NM_001318371.2 | 3 | 1413 | NP_001305300.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834175 | Chr.22:30580637 - 30693558 on Build GRCh38 | Gain |
 DUSP18
SLC35E4
PES1
TCN2
|
| nsv6549241 | Chr.22:30659456 - 30688376 on Build GRCh38 | Duplication |
DUSP18
SLC35E4
|
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Additional Information:
For this assay, SNP(s) [rs79182040] 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
|
Gene Ontology Categories:
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