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See other GLUD1 CNV Assays ›
Gene Symbol
GLUD1
Assay Reference Genome
Location

Chr.10:87062919 on build GRCh38
Cytoband
Assay ID Hs04375167_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 2746

Gene Name:

 glutamate dehydrogenase 1

Gene Aliases:

 GDH, GDH1, GLUD, hGDH1

Location:

 Chr.10:87050202-87094843 on Build GRCh38

Assay Gene Location:

 Within Intron 9
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_001318904.2 NP_001305833.1
NM_001318905.2 NP_001305834.1
NM_001318906.2 NP_001305835.1
NM_005271.5 NP_005262.1
XM_047425099.1 XP_047281055.1
XM_047425100.1 XP_047281056.1
AB209406.1 BAD92643.1
AK094782.1 BAG52930.1
AK122685.1 BAG53667.1
AK222818.1 BAD96538.1
AK294685.1 BAG57846.1
AK297441.1 BAG59867.1
AK297456.1 BAG59880.1
AK303458.1 BAG64501.1
AK311722.1
BC040132.1 AAH40132.1
BC112946.1 AAI12947.1
GQ891382.1 ADO22244.1
GU727646.1 ADU87647.1
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: 2025-12-01, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv6451688 Chr.10:87019399 - 87067528 on Build GRCh38 Duplication GLUD1 FAM25A
nsv428236 Chr.10:86866859 - 87550005 on Build GRCh38 Loss LINC00863 NUTM2A BMPR1A LOC124902474 MMRN2 FAM25A MIR4678 MINPP1 AGAP11 SNCG GLUD1 NUTM2D NUTM2A-AS1 FAM245A SHLD2 ADIRF-AS1 ADIRF
esv2759774 Chr.10:86755301 - 87550005 on Build GRCh38 Gain+Loss LINC00863 NUTM2A BMPR1A LOC124902474 MMRN2 FAM25A MIR4678 MINPP1 AGAP11 SNCG GLUD1 NUTM2D NUTM2A-AS1 FAM245A SHLD2 ADIRF-AS1 ADIRF
nsv831939 Chr.10:86984277 - 87154254 on Build GRCh38 Gain AGAP11 GLUD1 FAM25A SHLD2
nsv3216840 Chr.10:87062015 - 87073854 on Build GRCh38 Deletion GLUD1

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More 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

Gene Ontology Categories:

Function(s) Process(es)


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