Assay Details
Target Gene Details
Entrez Gene ID: | 219855 |
Gene Name: | solute carrier family 37 member 2 |
Gene Aliases: |
pp11662 |
Location: |
Chr.11:125063067-125090516 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC37A2 | NM_001145290.1 | NP_001138762.1 | ||
| NM_198277.2 | NP_938018.1 | |||
| AK074100.1 | BAB84926.1 | |||
| AK074207.1 | BAB85016.1 | |||
| AK290314.1 | ||||
| BC051314.1 | AAH51314.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1054682 | Chr.11:124971689 - 125071733 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs77844659] 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