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See other TMEM117 CNV Assays ›
Gene Symbol
TMEM117
Assay Reference Genome
Location

Chr.12:44146784 on build GRCh38
Cytoband
12q12
Assay ID Hs06352004_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 84216

Gene Name:

 transmembrane protein 117

Gene Aliases:

 -

Location:

 Chr.12:43795806-44389762 on Build GRCh38

Assay Gene Location:

 Within Intron 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TMEM117 NM_001286211.1 NP_001273140.1
NM_001286212.1 NP_001273141.1
NM_001286213.1 NP_001273142.1
NM_032256.2 NP_115632.1
XM_011538831.2 XP_011537133.1
XM_011538832.2 XP_011537134.1
XM_011538833.2 XP_011537135.1
XM_017020022.1 XP_016875511.1
XM_017020023.1 XP_016875512.1
AK057287.1 BAB71411.1
AL136855.1 CAB66789.1
BC030284.1
BC060798.1 AAH60798.1
DA007410.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv832391 Chr.12:44000334 - 44158752 on Build GRCh38 Loss TMEM117
nsv1049818 Chr.12:44092509 - 44740000 on Build GRCh38 Gain NELL2 TMEM117
nsv1051285 Chr.12:44054046 - 45582132 on Build GRCh38 Loss RACGAP1P NELL2 PLEKHA8P1 ANO6 DBX2 TMEM117
nsv832393 Chr.12:44135603 - 44298631 on Build GRCh38 Gain TMEM117

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More Information


Additional Information:

For this assay, SNP(s) [rs73290215] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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