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- Gene Symbol
- GRID1
- Assay Reference Genome
Location
Chr.10:85697599 on build GRCh38- Cytoband
Genomic Map
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Target Gene Details
Entrez Gene ID: | 2894 |
Gene Name: | glutamate ionotropic receptor delta type subunit 1 |
Gene Aliases: |
GluD1, GluD1-b |
Location: |
Chr.10:85599552-86366795 on Build GRCh38 |
Assay Gene Location: | Within Intron 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GRID1 | NM_017551.3 | NP_060021.1 | ||
| XM_047425122.1 | XP_047281078.1 | |||
| XM_047425123.1 | XP_047281079.1 | |||
| AB033046.1 | BAA86534.1 | |||
| AK127168.1 | BAG54447.1 | |||
| AK293104.1 | BAF85793.1 | |||
| AK302192.1 | BAH13646.1 | |||
| BC039263.1 | AAH39263.1 | |||
| BK014583.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1052427 | Chr.10:85234813 - 86270793 on Build GRCh38 | Gain |
 LINC01520
GRID1-AS1
GRID1-AS2
LOC101929662
GRID1
MIR346
LINC02647
|
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Additional Information:
For this assay, SNP(s) [rs73328612] 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
|
Gene Ontology Categories:
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