Genomic Map
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Target Gene Details
Entrez Gene ID: | 6547 |
Gene Name: | solute carrier family 8 member A3 |
Gene Aliases: |
NCX3 |
Location: |
Chr.14:70044217-70189626 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC8A3 | NM_001130417.2 | 6 | 1546 | NP_001123889.1 |
| NM_033262.4 | 8 | 3843 | NP_150287.1 | |
| NM_058240.3 | 8 | 3840 | NP_489479.1 | |
| NM_182932.2 | 7 | 3831 | NP_891977.1 | |
| NM_182936.2 | 5 | 1442 | NP_891981.1 | |
| NM_183002.2 | 8 | 3849 | NP_892114.1 | |
| NR_104122.1 | 6 | 3727 | ||
| XM_006720240.3 | 7 | 2695 | XP_006720303.1 | |
| XM_017021606.1 | 8 | 3221 | XP_016877095.1 | |
| XM_017021607.1 | 8 | 3711 | XP_016877096.1 | |
| XM_017021608.1 | 7 | 3457 | XP_016877097.1 | |
| XM_017021609.1 | 7 | 3693 | XP_016877098.1 | |
| XM_017021611.1 | 6 | 1819 | XP_016877100.1 | |
| AF510501.1 | 7 | 3831 | AAN60790.1 | |
| AF510502.1 | 8 | 3849 | AAN60791.1 | |
| AF510503.1 | 6 | 3727 | AAN60792.1 | |
| AJ508602.1 | 6 | 2627 | CAD48420.1 | |
| AJ745101.1 | 5 | 1405 | CAG33739.1 | |
| AJ745102.1 | 6 | 1509 | CAG33740.1 | |
| AK096553.1 | 5 | 1372 | ||
| AK122728.1 | 6 | 1533 | ||
| BC142969.1 | 6 | 1535 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv456336 | Chr.14:69615239 - 70107432 on Build GRCh38 | Gain |
 LOC100289511
SUSD6
SRSF5
SMOC1
LOC100506358
SLC8A3
SLC10A1
|
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Additional Information:
For this assay, SNP(s) [rs75876443] 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
|
Panther Classification:
Gene Ontology Categories:
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