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 TMEM259 CNV Assays ›
Gene Symbol
TMEM259
Assay Reference Genome
Location

Chr.19:1011947 on build GRCh38
Cytoband
19p13.3
Assay ID Hs00613480_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 91304

Gene Name:

 transmembrane protein 259

Gene Aliases:

 ASBABP1, C19orf6, MBRL, MEMBRALIN, R32184_3

Location:

 Chr.19:1009651-1021169 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 6 - Exon 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TMEM259 NM_001033026.1 NP_001028198.1
NM_033420.3 NP_219488.1
XM_005259675.2 XP_005259732.1
XM_005259676.2 XP_005259733.1
XM_005259677.2 XP_005259734.1
XM_005259678.2 XP_005259735.1
XM_017027457.1 XP_016882946.1
AK090400.1 BAC03381.1
AK095756.1
BC008957.2 AAH08957.1
DQ005958.1 AAY27747.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv9662 Chr.19:893394 - 1317740 on Build GRCh38 Gain STK11 RNU6-9 GPX4 SBNO2 LOC105372235 POLR2E CIRBP-AS1 GRIN3B LOC102725180 KISS1R CNN2 ARHGAP45 R3HDM4 CBARP ARID3A CIRBP EFNA2 MIDN TMEM259 RNU6-2 C19orf24 ABCA7 WDR18 ATP5D
nsv1160555 Chr.19:887275 - 1346084 on Build GRCh38 Deletion RNU6-9 MED16 GPX4 POLR2E CIRBP-AS1 GRIN3B KISS1R CNN2 CBARP ARID3A EFNA2 TMEM259 RNU6-2 C19orf24 WDR18 STK11 SBNO2 LOC105372235 LOC102725180 ARHGAP45 R3HDM4 CIRBP MIDN ABCA7 ATP5D
nsv578189 Chr.19:1007994 - 1013149 on Build GRCh38 Loss LOC105372235 GRIN3B TMEM259
nsv578188 Chr.19:923744 - 1059005 on Build GRCh38 Loss ARID3A LOC105372235 GRIN3B TMEM259 CNN2 RNU6-2 ABCA7 WDR18
nsv469845 Chr.19:951640 - 1144486 on Build GRCh38 Loss ARID3A GPX4 SBNO2 LOC105372235 POLR2E GRIN3B TMEM259 CNN2 RNU6-2 ARHGAP45 ABCA7 WDR18
nsv833704 Chr.19:951641 - 1144486 on Build GRCh38 Gain ARID3A GPX4 SBNO2 LOC105372235 POLR2E GRIN3B TMEM259 CNN2 RNU6-2 ARHGAP45 ABCA7 WDR18
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion RNU6-9 MED16 GPX4 POLR2E PRSS57 MADCAM1 PLPPR3 GRIN3B KISS1R CNN2 CDC34 POLRMT MIR4745 ARID3A HCN2 THEG TMEM259 PTBP1 RNU6-2 WDR18 MISP SHC2 LOC105372235 CFD PRTN3 TPGS1 ELANE ODF3L2 ARHGAP45 FGF22 R3HDM4 MIR3187 GZMM LOC101928450 RNF126 AZU1 BSG FSTL3 ABCA7 PALM C2CD4C

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs73497158] 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 Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


Back To Top

Related Products