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Gene Symbol
EMC4
Assay Reference Genome
Location

Chr.15:34229858 on build GRCh38
Cytoband
15q14
Assay ID Hs00432128_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 51234

Gene Name:

 ER membrane protein complex subunit 4

Gene Aliases:

 PIG17, TMEM85

Location:

 Chr.15:34224997-34230165 on Build GRCh38

Assay Gene Location:

 Within Exon 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
EMC4 NM_001286420.1 4 579 NP_001273349.1
NM_016454.3 5 740 NP_057538.1
AF151018.1 5 693 AAF36104.1
AK075227.1 5 719 BAC11486.1
AK290524.1 4 563
BC002583.2 4 544 AAH02583.1
BG707804.1
DB506932.1 2 151
KU178640.1
KU178641.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1052620 Chr.15:32612402 - 34538731 on Build GRCh38 Gain NOP10 CHRM5 AVEN GOLGA8B PGBD4 LOC101928134 GREM1 LOC101928042 LOC100131315 RYR3 LOC105370757 KATNBL1 LPCAT4 SLC12A6 FMN1 EMC4 MIR1233-1 NUTM1 MIR1233-2 ARHGAP11A TMCO5B GOLGA8A SCG5 EMC7
esv33337 Chr.15:31689863 - 34575097 on Build GRCh38 Gain+Loss ULK4P1 CHRM5 AVEN PGBD4 LOC100996255 LOC100131315 RYR3 KATNBL1 LOC100653133 EMC4 GOLGA8A CHRNA7 GOLGA8O EMC7 NOP10 LOC101060588 WHAMMP1 GOLGA8B LOC101928134 GREM1 GOLGA8N LOC101928042 LOC105370757 LPCAT4 SLC12A6 FMN1 MIR1233-1 NUTM1 MIR1233-2 ARHGAP11A TMCO5B SCG5 LOC105370940 GOLGA8K
esv3569431 Chr.15:33564570 - 35080307 on Build GRCh38 Gain NOP10 CHRM5 AVEN ACTC1 LOC101928174 GOLGA8B PGBD4 GJD2 ZNF770 RYR3 KATNBL1 LPCAT4 SLC12A6 EMC4 MIR1233-1 NUTM1 MIR1233-2 AQR GOLGA8A EMC7
dgv4456n54 Chr.15:32604149 - 34557061 on Build GRCh38 Gain CHRM5 AVEN PGBD4 LOC100131315 RYR3 KATNBL1 EMC4 GOLGA8A EMC7 NOP10 GOLGA8B LOC101928134 GREM1 GOLGA8N LOC101928042 LOC105370757 LPCAT4 SLC12A6 FMN1 MIR1233-1 NUTM1 MIR1233-2 ARHGAP11A TMCO5B SCG5

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More Information


Additional Information:

For this assay, SNP(s) [rs71702457] 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 Exonic DGV Variation

Gene Ontology Categories:

Function(s)


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