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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
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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 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 SBNO2 ATP5D KISS1R CBARP STK11 TMEM259 POLR2E R3HDM4 CNN2 ARID3A RNU6-2 LOC105372235 RNU6-9 C19orf24 MIDN EFNA2 CIRBP-AS1 GRIN3B ABCA7 CIRBP ARHGAP45 GPX4 WDR18 LOC102725180
nsv1160555 Chr.19:887275 - 1346084 on Build GRCh38 Deletion SBNO2 ATP5D TMEM259 POLR2E CNN2 RNU6-2 LOC105372235 RNU6-9 MED16 EFNA2 ABCA7 CIRBP ARHGAP45 WDR18 KISS1R CBARP STK11 R3HDM4 ARID3A C19orf24 MIDN CIRBP-AS1 GRIN3B GPX4 LOC102725180
nsv578189 Chr.19:1007994 - 1013149 on Build GRCh38 Loss TMEM259 GRIN3B LOC105372235
nsv578188 Chr.19:923744 - 1059005 on Build GRCh38 Loss TMEM259 GRIN3B ABCA7 CNN2 ARID3A RNU6-2 LOC105372235 WDR18
nsv469845 Chr.19:951640 - 1144486 on Build GRCh38 Loss SBNO2 TMEM259 POLR2E GRIN3B ABCA7 CNN2 ARID3A ARHGAP45 GPX4 RNU6-2 LOC105372235 WDR18
esv2758743 Chr.19:951641 - 1544934 on Build GRCh38 Gain+Loss SBNO2 ATP5D TMEM259 POLR2E PLK5 CNN2 RNU6-2 LOC105372235 GAMT REEP6 EFNA2 ABCA7 CIRBP ARHGAP45 WDR18 APC2 CBARP STK11 ARID3A PCSK4 DAZAP1 C19orf24 C19orf25 MIDN CIRBP-AS1 GRIN3B RPS15 MUM1 GPX4 NDUFS7 LOC102725180 ADAMTSL5
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion TMEM259 POLR2E GZMM HCN2 CFD POLRMT CNN2 RNU6-2 LOC105372235 RNU6-9 MIR4745 FGF22 MED16 ABCA7 PALM ARHGAP45 THEG WDR18 CDC34 C2CD4C KISS1R TPGS1 R3HDM4 ARID3A MIR3187 MISP LOC101928450 PTBP1 ELANE BSG PLPPR3 SHC2 PRTN3 GRIN3B PRSS57 GPX4 RNF126 AZU1 ODF3L2 FSTL3 MADCAM1

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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)


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