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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 ARHGAP45 ABCA7 POLR2E CBARP ATP5D RNU6-2 CIRBP STK11 R3HDM4 GRIN3B LOC102725180 CNN2 CIRBP-AS1 RNU6-9 ARID3A SBNO2 EFNA2 GPX4 KISS1R C19orf24 TMEM259 LOC105372235 MIDN WDR18
nsv1160555 Chr.19:887275 - 1346084 on Build GRCh38 Deletion ARHGAP45 ABCA7 POLR2E ATP5D CIRBP STK11 GRIN3B CNN2 CIRBP-AS1 ARID3A SBNO2 KISS1R MED16 LOC105372235 CBARP RNU6-2 R3HDM4 LOC102725180 RNU6-9 EFNA2 GPX4 C19orf24 TMEM259 MIDN WDR18
nsv578189 Chr.19:1007994 - 1013149 on Build GRCh38 Loss TMEM259 LOC105372235 GRIN3B
nsv578188 Chr.19:923744 - 1059005 on Build GRCh38 Loss CNN2 ARID3A ABCA7 RNU6-2 TMEM259 LOC105372235 GRIN3B WDR18
esv3643383 Chr.19:1012555 - 1069137 on Build GRCh38 Gain ARHGAP45 CNN2 ABCA7 RNU6-2 TMEM259
nsv469845 Chr.19:951640 - 1144486 on Build GRCh38 Loss ARHGAP45 CNN2 ARID3A SBNO2 ABCA7 POLR2E RNU6-2 GPX4 TMEM259 LOC105372235 GRIN3B WDR18
nsv833704 Chr.19:951641 - 1144486 on Build GRCh38 Gain ARHGAP45 CNN2 ARID3A SBNO2 ABCA7 POLR2E RNU6-2 GPX4 TMEM259 LOC105372235 GRIN3B WDR18
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion ARHGAP45 FSTL3 ABCA7 THEG AZU1 POLR2E C2CD4C GRIN3B MISP MIR3187 GZMM CNN2 MADCAM1 ARID3A RNF126 PRTN3 FGF22 KISS1R MED16 LOC105372235 TPGS1 PLPPR3 PRSS57 PTBP1 BSG RNU6-2 R3HDM4 CFD ELANE HCN2 RNU6-9 PALM MIR4745 SHC2 POLRMT GPX4 ODF3L2 TMEM259 LOC101928450 CDC34 WDR18

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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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