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See other MROH5 CNV Assays ›
Gene Symbol
MROH5
Assay Reference Genome
Location

Chr.8:141439843 on build GRCh38
Cytoband
8q24.3
Assay ID Hs03696961_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 389690

Gene Name:

 maestro heat like repeat family member 5

Gene Aliases:

 -

Location:

 Chr.8:141433829-141507230 on Build GRCh38

Assay Gene Location:

 Within Intron 25
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MROH5 NM_207414.2 NP_997297.2
NR_102363.2
NR_102364.2
AK125848.1 BAC86317.1
AK131461.1 BAD18606.1
DN831584.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv470240 Chr.8:141294623 - 141513653 on Build GRCh38 Loss FP248 SLC45A4 LINC01300 PTP4A3 MROH5 GPR20
nsv949996 Chr.8:141306802 - 141672500 on Build GRCh38 Deletion FP248 SLC45A4 LINC01300 PTP4A3 MROH5 GPR20
nsv509285 Chr.8:141306491 - 141505253 on Build GRCh38 Insertion FP248 SLC45A4 LINC01300 PTP4A3 MROH5 GPR20
esv2737756 Chr.8:140419230 - 141917755 on Build GRCh38 Deletion FP248 DENND3 LOC107986982 AGO2 CHRAC1 LOC105375787 MROH5 MIR1302-7 PTK2 SLC45A4 LINC01300 MIR151A PTP4A3 TRAPPC9 GPR20
nsv612577 Chr.8:141326581 - 141448932 on Build GRCh38 Loss FP248 LINC01300 PTP4A3 MROH5 GPR20
dgv7331n100 Chr.8:141316334 - 141451594 on Build GRCh38 Gain FP248 LINC01300 PTP4A3 MROH5 GPR20
dgv12368n54 Chr.8:141423157 - 141457475 on Build GRCh38 Loss FP248 PTP4A3 MROH5
nsv1126125 Chr.8:140419236 - 141917668 on Build GRCh38 Deletion FP248 DENND3 LOC107986982 AGO2 CHRAC1 LOC105375787 MROH5 MIR1302-7 PTK2 SLC45A4 LINC01300 MIR151A PTP4A3 TRAPPC9 GPR20
nsv1023036 Chr.8:141348766 - 141497430 on Build GRCh38 Loss FP248 PTP4A3 MROH5 GPR20

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More Information


Additional Information:

For this assay, SNP(s) [rs116005707] 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

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