Assay Details
Target Gene Details
Entrez Gene ID: | 87769 |
Gene Name: | gamma-glutamylamine cyclotransferase |
Gene Aliases: |
A2LD1 |
Location: |
Chr.13:100530164-100588792 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GGACT | NM_001195087.1 | 3 | 2380 | NP_001182016.1 |
| NM_033110.2 | 2 | 2395 | NP_149101.1 | |
| XM_005254083.2 | 2 | 2522 | XP_005254140.1 | |
| XM_011521129.2 | 3 | 5358 | XP_011519431.1 | |
| XM_017020804.1 | 3 | 2496 | XP_016876293.1 | |
| AK091974.1 | 3 | 2068 | ||
| AK093228.1 | 1 | 1611 | ||
| AK095850.1 | 3 | 2380 |
Target Gene Details
Entrez Gene ID: | 5095 |
Gene Name: | propionyl-CoA carboxylase alpha subunit |
Gene Aliases: |
- |
Location: |
Chr.13:100089015-100530437 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 33 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PCCA | NM_000282.3 | NP_000273.2 | ||
| NM_001127692.2 | NP_001121164.1 | |||
| NM_001178004.1 | NP_001171475.1 | |||
| XM_017020608.1 | XP_016876097.1 | |||
| XM_017020609.1 | XP_016876098.1 | |||
| XM_017020613.1 | XP_016876102.1 | |||
| XM_017020614.1 | XP_016876103.1 | |||
| XM_017020617.1 | XP_016876106.1 | |||
| XM_017020618.1 | XP_016876107.1 | |||
| AF385926.1 | AAL66189.1 | |||
| AK225288.1 | ||||
| AK296771.1 | ||||
| BC000140.2 | AAH00140.1 | |||
| CB851764.1 | ||||
| S79219.1 | AAB35181.1 | |||
| X14608.1 | CAA32763.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1037414 | Chr.13:100521000 - 100622872 on Build GRCh38 | Loss |
|
| esv3582760 | Chr.13:100471360 - 100566346 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs201062235] 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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Genomic Map