accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other ALDH3A1 CNV Assays ›
Gene Symbol
ALDH3A1
Assay Reference Genome
Location

Chr.17:19743730 on build GRCh38
Cytoband
17p11.2
Assay ID Hs03986856_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 218

Gene Name:

 aldehyde dehydrogenase 3 family member A1

Gene Aliases:

 ALDH3, ALDHIII

Location:

 Chr.17:19737984-19748433 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ALDH3A1 NM_000691.4 NP_000682.3
NM_001135167.1 NP_001128639.1
NM_001135168.1 NP_001128640.1
XM_005256522.1 XP_005256579.1
XM_005256523.2 XP_005256580.1
XM_005256524.3 XP_005256581.1
XM_011523730.1 XP_011522032.1
XM_011523731.1 1 678 XP_011522033.1
AK091272.1 1 678
AK093755.1 1 1039
AK093877.1 BAC04239.1
AK225505.1
AK225513.1
AK292193.1
AK314584.1
BC004102.2 AAH04102.1
BC004370.1 AAH04370.1
BC008892.2 AAH08892.1
BC021194.2 AAH21194.1
BM979497.1
BT007102.1 AAP35766.1
DA427150.1
M74542.1 AAA51696.1
M77477.1 AAB46377.1
S61044.1 AAB26658.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1063892 Chr.17:19661321 - 19905172 on Build GRCh38 Gain ALDH3A1 ALDH3A2 ULK2 SLC47A2 AKAP10
nsv470582 Chr.17:19717164 - 19760434 on Build GRCh38 Loss ALDH3A1 SLC47A2
nsv953846 Chr.17:19738588 - 19750287 on Build GRCh38 Deletion ALDH3A1
nsv526290 Chr.17:19710044 - 19748169 on Build GRCh38 Loss ALDH3A1 SLC47A2
nsv1061317 Chr.17:19047542 - 20322438 on Build GRCh38 Gain GRAP ULK2 ALDH3A1 GRAPL SNORD3B-1 SNORD3D SPECC1 SNORD3B-2 SLC47A2 LOC79999 MAPK7 SLC47A1 B9D1 EPN2-AS1 AKAP10 EPN2 LOC388436 EPN2-IT1 SNORD3A SNORD3C RPS2P46 MIR1180 ALDH3A2 LOC102724624 SNORA59B RNF112 LOC100131943 MFAP4 CCDC144CP

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs143739303] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

dehydrogenase

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products