Assay Details
Target Gene Details
Entrez Gene ID: | 285641 |
Gene Name: | solute carrier family 36 member 3 |
Gene Aliases: |
PAT3, TRAMD2, tramdorin2 |
Location: |
Chr.5:151276365-151303773 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC36A3 | NM_001145017.1 | NP_001138489.1 | ||
NM_181774.3 | NP_861439.3 | |||
XM_011537627.2 | XP_011535929.1 | |||
XM_011537629.2 | XP_011535931.1 | |||
XM_011537630.1 | XP_011535932.1 | |||
XM_011537631.1 | XP_011535933.1 | |||
XM_011537633.1 | XP_011535935.1 | |||
AK127978.1 | BAC87215.1 | |||
AK131483.1 | BAD18628.1 | |||
AY162215.1 | AAO11789.1 | |||
AY228365.1 | ||||
BC101092.1 | AAI01093.1 | |||
BC101093.1 | AAI01094.1 | |||
BC101094.1 | AAI01095.1 | |||
BC101095.2 | AAI01096.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1032558 | Chr.5:151257308 - 151325163 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs75985776] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)