Assay Details
Target Gene Details
Entrez Gene ID: | 10006 |
Gene Name: | abl interactor 1 |
Gene Aliases: |
ABI-1, ABLBP4, E3B1, NAP1BP, SSH3BP, SSH3BP1 |
Location: |
Chr.10:26746596-26861087 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ABI1 | NM_001012750.2 | 11 | 3431 | NP_001012768.1 |
NM_001012751.2 | 10 | 3344 | NP_001012769.1 | |
NM_001012752.2 | 10 | 3416 | NP_001012770.1 | |
NM_001178116.1 | 12 | 3476 | NP_001171587.1 | |
NM_001178119.1 | 11 | 3428 | NP_001171590.1 | |
NM_001178120.1 | 10 | 3341 | NP_001171591.1 | |
NM_001178121.1 | 9 | 3326 | NP_001171592.1 | |
NM_001178122.1 | 10 | 3254 | NP_001171593.1 | |
NM_001178123.1 | 9 | 3167 | NP_001171594.1 | |
NM_001178124.1 | 8 | 3152 | NP_001171595.1 | |
NM_001178125.1 | 7 | 2975 | NP_001171596.1 | |
NM_005470.3 | 12 | 3512 | NP_005461.2 |
Target Gene Details
Entrez Gene ID: | 23590 |
Gene Name: | prenyl (decaprenyl) diphosphate synthase, subunit 1 |
Gene Aliases: |
COQ1, COQ10D2, DPS, SPS, TPRT, TPT, TPT 1, hDPS1 |
Location: |
Chr.10:26697052-26746798 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PDSS1 | NM_001321978.1 | NP_001308907.1 | ||
NM_001321979.1 | NP_001308908.1 | |||
NM_014317.4 | NP_055132.2 | |||
XM_011519437.2 | XP_011517739.1 | |||
XM_017016011.1 | XP_016871500.1 | |||
AB209763.1 | BAD93000.1 | |||
AB210838.1 | BAE48216.1 | |||
AF118395.1 | AAD28559.1 | |||
AK024802.1 | ||||
AK223414.1 | BAD97134.1 | |||
AK296288.1 | 5 | 942 | ||
BC049211.1 | AAH49211.1 | |||
BC063635.1 | AAH63635.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3415799 | Chr.10:26640952 - 26944612 on Build GRCh38 | Duplication | LINC00202-1 ABI1 LINC00202-2 PDSS1 ANKRD26 |
More Information
Additional Information:
For this assay, SNP(s) [rs74547466] 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 Non-exonic DGV Variation |