Assay Details
Target Gene Details
Entrez Gene ID: | 64849 |
Gene Name: | solute carrier family 13 member 3 |
Gene Aliases: |
NADC3, SDCT2 |
Location: |
Chr.20:46557823-46684485 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC13A3 | NM_001011554.2 | 14 | 2967 | NP_001011554.1 |
NM_001193339.1 | 12 | 2781 | NP_001180268.1 | |
NM_001193340.1 | 13 | 2862 | NP_001180269.1 | |
NM_001193342.1 | 13 | 2758 | NP_001180271.1 | |
NM_022829.5 | 13 | 2931 | NP_073740.2 | |
AF154121.1 | 13 | 2910 | AAF73251.1 | |
AK056713.1 | 13 | 2929 | BAB71262.1 | |
AK096658.1 | 13 | 2862 | BAC04834.1 | |
AK123351.1 | 2 | 1555 | ||
AL442082.1 | 4 | 1595 | CAC09447.2 | |
AY072810.3 | 13 | 2910 | AAL66762.1 | |
BC035966.1 | 13 | 2929 | AAH35966.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833994 | Chr.20:46442116 - 46680210 on Build GRCh38 | Gain | LOC105372633 ZNF663P ZNF334 SLC13A3 OCSTAMP MKRN7P |
nsv1061899 | Chr.20:46498425 - 47439490 on Build GRCh38 | Loss | LOC101927377 LOC100131496 ZNF334 SLC2A10 SLC13A3 OCSTAMP EYA2 TP53RK MIR3616 ZMYND8 |
More Information
Additional Information:
For this assay, SNP(s) [rs79071072] 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 DGV Variation |