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See other TMEM259 CNV Assays ›
Gene Symbol
TMEM259
Assay Reference Genome
Location

Chr.19:1012587 on build GRCh38
Cytoband
19p13.3
Assay ID Hs02431186_cn
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Availability Made To Order
Catalog # 4400291
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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 3 - Exon 4
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
AK095756.1
BC008957.2 AAH08957.1
BQ895919.1
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 CIRBP C19orf24 MIDN ARHGAP45 POLR2E EFNA2 CNN2 R3HDM4 CIRBP-AS1 KISS1R ARID3A SBNO2 ATP5D WDR18 LOC105372235 GRIN3B TMEM259 RNU6-2 GPX4 RNU6-9 ABCA7 LOC102725180 CBARP
nsv1160555 Chr.19:887275 - 1346084 on Build GRCh38 Deletion STK11 C19orf24 ARHGAP45 POLR2E EFNA2 CNN2 KISS1R RNU6-2 ABCA7 CBARP CIRBP MIDN R3HDM4 MED16 CIRBP-AS1 ARID3A SBNO2 ATP5D WDR18 LOC105372235 GRIN3B TMEM259 GPX4 RNU6-9 LOC102725180
nsv578189 Chr.19:1007994 - 1013149 on Build GRCh38 Loss LOC105372235 GRIN3B TMEM259
esv3643383 Chr.19:1012555 - 1069137 on Build GRCh38 Gain ARHGAP45 CNN2 TMEM259 RNU6-2 ABCA7
nsv578188 Chr.19:923744 - 1059005 on Build GRCh38 Loss WDR18 LOC105372235 GRIN3B CNN2 TMEM259 RNU6-2 ABCA7 ARID3A
nsv469845 Chr.19:951640 - 1144486 on Build GRCh38 Loss WDR18 LOC105372235 GRIN3B ARHGAP45 POLR2E CNN2 TMEM259 RNU6-2 GPX4 ABCA7 ARID3A SBNO2
esv2758743 Chr.19:951641 - 1544934 on Build GRCh38 Gain+Loss STK11 C19orf24 ARHGAP45 POLR2E EFNA2 CNN2 REEP6 APC2 PLK5 GAMT RNU6-2 MUM1 PCSK4 ABCA7 CBARP RPS15 CIRBP MIDN C19orf25 CIRBP-AS1 ARID3A SBNO2 ATP5D WDR18 LOC105372235 GRIN3B TMEM259 ADAMTSL5 DAZAP1 GPX4 LOC102725180 NDUFS7
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion SHC2 CDC34 THEG PTBP1 FGF22 ARHGAP45 POLR2E CNN2 RNF126 PLPPR3 MADCAM1 KISS1R CFD MIR4745 TPGS1 LOC101928450 PRSS57 ELANE MIR3187 RNU6-2 ODF3L2 ABCA7 GZMM FSTL3 PRTN3 BSG R3HDM4 MED16 ARID3A MISP WDR18 POLRMT AZU1 LOC105372235 GRIN3B TMEM259 HCN2 C2CD4C GPX4 RNU6-9 PALM

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More Information


Additional Information:

For this assay, SNP(s) [rs71335287] 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)


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