Assay Details
Target Gene Details
Entrez Gene ID: | 9546 |
Gene Name: | amyloid beta precursor protein binding family A member 3 |
Gene Aliases: |
MGC:15815, X11L2, mint3 |
Location: |
Chr.19:3750773-3761697 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APBA3 | NM_004886.3 | NP_004877.1 | ||
XM_006722950.3 | XP_006723013.1 | |||
XM_006722951.3 | XP_006723014.1 | |||
AB021638.1 | BAA74430.1 | |||
AB209603.1 | 1 | 377 | BAD92840.1 | |
BC086306.1 | AAH86306.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv509718 | Chr.19:3676947 - 3844683 on Build GRCh38 | Insertion | RAX2 ZFR2 MATK MRPL54 APBA3 PIP5K1C TJP3 |
nsv470114 | Chr.19:3372516 - 3855979 on Build GRCh38 | Loss | RAX2 MFSD12 HMG20B C19orf71 MRPL54 CACTIN PIP5K1C DOHH TJP3 CACTIN-AS1 SMIM24 GIPC3 ZFR2 TBXA2R MATK FZR1 APBA3 NFIC |
More Information
Additional Information:
For this assay, SNP(s) [rs113573788] 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 |