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 Intron 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC8A3 | NM_001130417.2 | NP_001123889.1 | ||
| NM_033262.4 | NP_150287.1 | |||
| NM_058240.3 | NP_489479.1 | |||
| NM_182932.2 | NP_891977.1 | |||
| NM_182936.2 | NP_891981.1 | |||
| NM_183002.2 | NP_892114.1 | |||
| NR_104122.1 | ||||
| XM_006720240.3 | XP_006720303.1 | |||
| XM_017021606.1 | XP_016877095.1 | |||
| XM_017021607.1 | XP_016877096.1 | |||
| XM_017021608.1 | XP_016877097.1 | |||
| XM_017021609.1 | XP_016877098.1 | |||
| XM_017021611.1 | XP_016877100.1 | |||
| AF510501.1 | AAN60790.1 | |||
| AF510502.1 | AAN60791.1 | |||
| AF510503.1 | AAN60792.1 | |||
| AJ304852.1 | CAC40984.1 | |||
| AJ304853.1 | CAC40985.1 | |||
| AJ508602.1 | CAD48420.1 | |||
| AJ745101.1 | CAG33739.1 | |||
| AJ745102.1 | CAG33740.1 | |||
| AK096553.1 | ||||
| AK122728.1 | ||||
| BC142969.1 | ||||
| BC150183.1 | ||||
| BC150193.1 |
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 |
 SLC10A1
SLC8A3
SUSD6
SRSF5
LOC100506358
LOC100289511
SMOC1
|
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Additional Information:
For this assay, SNP(s) [rs138244766,rs73292509] 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
|
Panther Classification:
Gene Ontology Categories:
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