Assay Details
Target Gene Details
Entrez Gene ID: | 57210 |
Gene Name: | solute carrier family 45 member 4 |
Gene Aliases: |
- |
Location: |
Chr.8:141207166-141308321 on Build GRCh38 |
Assay Gene Location: | Within Intron 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC45A4 | NM_001080431.2 | NP_001073900.1 | ||
| NM_001286646.1 | NP_001273575.1 | |||
| NM_001286648.1 | NP_001273577.1 | |||
| XM_011517169.2 | XP_011515471.1 | |||
| XM_011517170.2 | XP_011515472.1 | |||
| XM_011517171.2 | XP_011515473.1 | |||
| XM_011517172.2 | XP_011515474.1 | |||
| XM_011517173.2 | XP_011515475.1 | |||
| XM_011517174.2 | XP_011515476.1 | |||
| XM_011517176.2 | XP_011515478.1 | |||
| XM_011517177.2 | XP_011515479.1 | |||
| XM_011517178.2 | XP_011515480.1 | |||
| XM_011517179.2 | XP_011515481.1 | |||
| XM_017013648.1 | XP_016869137.1 | |||
| XM_017013649.1 | XP_016869138.1 | |||
| XM_017013650.1 | XP_016869139.1 | |||
| AB032952.1 | BAA86440.1 | |||
| AK128212.1 | BAC87328.1 | |||
| BC090891.1 | AAH90891.1 | |||
| BC157840.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv6428 | Chr.8:141211968 - 141245531 on Build GRCh38 | Insertion |
|
| nsv470239 | Chr.8:141182470 - 141231139 on Build GRCh38 | Loss |
|
| esv2737756 | Chr.8:140419230 - 141917755 on Build GRCh38 | Deletion |
|
| nsv1019363 | Chr.8:141195805 - 141236451 on Build GRCh38 | Gain |
|
| nsv612568 | Chr.8:140534649 - 141326581 on Build GRCh38 | Gain |
|
| nsv612573 | Chr.8:141212346 - 141252228 on Build GRCh38 | Gain |
|
| nsv516666 | Chr.8:141209711 - 141231139 on Build GRCh38 | Loss |
|
| nsv831483 | Chr.8:141123462 - 141290370 on Build GRCh38 | Gain |
|
| nsv949995 | Chr.8:141211502 - 141233101 on Build GRCh38 | Deletion |
|
| nsv1126125 | Chr.8:140419236 - 141917668 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs75010825] 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: |
|

Genomic Map