Assay Details
Target Gene Details
Entrez Gene ID: | 320 |
Gene Name: | amyloid beta precursor protein binding family A member 1 |
Gene Aliases: |
D9S411E, LIN10, MINT1, X11, X11A, X11ALPHA |
Location: |
Chr.9:69427532-69673012 on Build GRCh38 |
Assay Gene Location: | Within Intron 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APBA1 | NM_001163.3 | NP_001154.2 | ||
XM_005251968.3 | XP_005252025.1 | |||
XM_011518617.2 | XP_011516919.1 | |||
XM_017014670.1 | XP_016870159.1 | |||
AF029106.1 | AAC05304.1 | |||
AF047347.1 | AAC39766.1 | |||
L04953.1 | AAA61307.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv6551 | Chr.9:69432857 - 69446481 on Build GRCh38 | Insertion | APBA1 |
dgv7668n100 | Chr.9:69381047 - 69564931 on Build GRCh38 | Gain | FAM189A2 APBA1 |
nsv1039966 | Chr.9:69442388 - 69566648 on Build GRCh38 | Gain | APBA1 |
dgv7670n100 | Chr.9:69417465 - 69454398 on Build GRCh38 | Gain | APBA1 |
More Information
Additional Information:
For this assay, SNP(s) [rs139229517,rs146143426] 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 Intronic Non-exonic DGV Variation |