Assay Details
Target Gene Details
Entrez Gene ID: | 84561 |
Gene Name: | solute carrier family 12 member 8 |
Gene Aliases: |
CCC9 |
Location: |
Chr.3:125082636-125212765 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC12A8 | NM_001195483.1 | NP_001182412.1 | ||
NM_024628.5 | NP_078904.3 | |||
AF345197.1 | AAO49174.1 | |||
AF390442.1 | AAM73657.1 | |||
AK026841.1 | BAB15571.1 | |||
AK123001.1 | ||||
AK308484.1 | ||||
BC020506.1 | AAH20506.1 | |||
BC063528.1 | AAH63528.1 | |||
BC126158.1 | ||||
BC126160.1 | ||||
BX538023.1 | CAD97969.1 | |||
CR457363.1 | CAG33644.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv3982 | Chr.3:125078149 - 125106568 on Build GRCh38 | Insertion |
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esv34126 | Chr.3:125045570 - 125149965 on Build GRCh38 | Loss |
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nsv10311 | Chr.3:125073408 - 125703762 on Build GRCh38 | Gain |
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nsv1160974 | Chr.3:124577493 - 125300995 on Build GRCh38 | Duplication |
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nsv1001677 | Chr.3:124015843 - 125108694 on Build GRCh38 | Loss |
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nsv829712 | Chr.3:125038838 - 125183948 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs149354196,rs78669310] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)