Assay Details
Target Gene Details
Entrez Gene ID: | 8034 |
Gene Name: | solute carrier family 25 member 16 |
Gene Aliases: |
D10S105E, GDA, GDC, HGT.1, ML7, hML7 |
Location: |
Chr.10:68479961-68527523 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A16 | NM_001324312.1 | NP_001311241.1 | ||
NM_001324313.1 | NP_001311242.1 | |||
NM_001324314.1 | NP_001311243.1 | |||
NM_001324315.1 | NP_001311244.1 | |||
NM_001324317.1 | NP_001311246.1 | |||
NM_152707.3 | NP_689920.1 | |||
NR_136737.1 | ||||
XM_011540211.2 | XP_011538513.1 | |||
XM_017016695.1 | XP_016872184.1 | |||
AK123772.1 | ||||
AK290255.1 | ||||
AK295287.1 | ||||
AK298510.1 | ||||
BC030266.1 | AAH30266.1 | |||
M31659.1 | AAA36329.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1037679 | Chr.10:68493125 - 68695174 on Build GRCh38 | Gain |
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nsv948047 | Chr.10:68499326 - 68502449 on Build GRCh38 | Duplication |
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esv2762871 | Chr.10:68441880 - 68510208 on Build GRCh38 | Gain |
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dgv919n100 | Chr.10:68400084 - 68752800 on Build GRCh38 | Gain |
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nsv1044477 | Chr.10:68428357 - 68628622 on Build GRCh38 | Gain |
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nsv551434 | Chr.10:68384017 - 68503822 on Build GRCh38 | Loss |
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nsv1047983 | Chr.10:68414663 - 68849311 on Build GRCh38 | Gain |
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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) [rs141408384] 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)