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- Gene Symbol
- GLUD1
- Assay Reference Genome
Location
Chr.10:87062919 on build GRCh38- Cytoband
- 10q23.2
Genomic Map
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Target Gene Details
Entrez Gene ID: | 2746 |
Gene Name: | glutamate dehydrogenase 1 |
Gene Aliases: |
GDH, GDH1, GLUD |
Location: |
Chr.10:87050202-87095047 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GLUD1 | NM_001318900.1 | NP_001305829.1 | ||
| NM_001318901.1 | NP_001305830.1 | |||
| NM_001318902.1 | NP_001305831.1 | |||
| NM_001318904.1 | NP_001305833.1 | |||
| NM_001318905.1 | NP_001305834.1 | |||
| NM_001318906.1 | NP_001305835.1 | |||
| NM_005271.4 | NP_005262.1 | |||
| AB209406.1 | BAD92643.1 | |||
| AK094782.1 | ||||
| AK122685.1 | ||||
| AK222818.1 | BAD96538.1 | |||
| AK294685.1 | ||||
| AK297441.1 | ||||
| AK297456.1 | ||||
| AK303458.1 | ||||
| AK311722.1 | ||||
| BC040132.1 | AAH40132.1 | |||
| BC112946.1 | AAI12947.1 | |||
| GU727646.1 | ||||
| J03248.1 | AAA52523.1 | |||
| M20867.1 | AAA52526.1 | |||
| M37154.1 | AAA52525.1 | |||
| X07674.1 | CAA30521.1 | |||
| X07769.1 | CAA30598.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428236 | Chr.10:86866859 - 87550005 on Build GRCh38 | Loss |
 NUTM2D
ADIRF
LINC00864
MIR4678
GLUD1
MINPP1
FAM35A
MMRN2
AGAP11
LINC00863
SNCG
FAM25A
NUTM2A
NUTM2A-AS1
BMPR1A
|
| esv2759774 | Chr.10:86755301 - 87550005 on Build GRCh38 | Gain+Loss |
NUTM2D
ADIRF
LINC00864
MIR4678
GLUD1
MINPP1
FAM35A
MMRN2
AGAP11
LINC00863
SNCG
FAM25A
NUTM2A
NUTM2A-AS1
BMPR1A
|
| nsv831939 | Chr.10:86984277 - 87154254 on Build GRCh38 | Gain |
FAM35A
AGAP11
GLUD1
FAM25A
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs114657546] 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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