Assay Details
Target Gene Details
Entrez Gene ID: | 6512 |
Gene Name: | solute carrier family 1 member 7 |
Gene Aliases: |
AAAT, EAAT5 |
Location: |
Chr.1:53087179-53142632 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC1A7 | NM_001287595.1 | NP_001274524.1 | ||
NM_001287596.1 | NP_001274525.1 | |||
NM_001287597.1 | NP_001274526.1 | |||
NM_006671.5 | NP_006662.3 | |||
NR_109858.1 | ||||
AB593059.1 | ||||
AB593060.1 | ||||
AB593061.1 | ||||
BC000651.2 | AAH00651.1 | |||
BC012119.1 | AAH12119.1 | |||
BC017242.2 | AAH17242.1 | |||
JF917096.1 | ||||
U76362.1 | AAB53971.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1003159 | Chr.1:53079580 - 53117512 on Build GRCh38 | Gain |
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nsv1010121 | Chr.1:52939995 - 53134678 on Build GRCh38 | Gain |
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nsv546240 | Chr.1:53084515 - 53134406 on Build GRCh38 | Loss |
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nsv950739 | Chr.1:53061429 - 53136228 on Build GRCh38 | Deletion |
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nsv1001535 | Chr.1:52620368 - 53346539 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs80121951] 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:
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