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Gene Symbol
PML
Assay Reference Genome
Location

Chr.15:74020215 on build GRCh38
Cytoband
15q24.1
Assay ID Hs03907909_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
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Online offer:
4505.0
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Assay Details

Target Gene Details

Entrez Gene ID:

 5371

Gene Name:

 promyelocytic leukemia

Gene Aliases:

 MYL, PP8675, RNF71, TRIM19

Location:

 Chr.15:73994673-74047819 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PML NM_002675.3 NP_002666.1
NM_033238.2 NP_150241.2
NM_033239.2 NP_150242.1
NM_033240.2 NP_150243.2
NM_033244.3 NP_150247.2
NM_033246.2 NP_150249.1
NM_033247.2 NP_150250.2
NM_033249.2 NP_150252.1
NM_033250.2 NP_150253.2
AB208950.1 BAD92187.1
AB209051.1 BAD92288.1
AB209411.1 BAD92648.1
AF230401.1 AAG50180.1
AF230402.1 AAG50181.1
AF230403.1 AAG50182.1
AF230404.1 AAG50183.1
AF230405.1 AAG50184.1
AF230406.1 AAG50185.1
AF230407.1 AAG50186.1
AF230408.1 AAG50187.1
AF230409.1 AAG50188.1
AF230410.1 AAG50189.1
AF230411.1 AAG50190.1
AK300256.1
AK300951.1
BC000080.2 AAH00080.2
BC020994.2 AAH20994.1
BT009911.1 AAP88913.1
M73778.1 AAA60125.1
M79462.1 AAA60388.1
M79463.1 AAA60351.1
M79464.1 AAA60390.1
M80185.1 AAA60352.1
S50913.1 AAB19601.2
X63131.1 CAA44841.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv457203 Chr.15:74016599 - 74055382 on Build GRCh38 Loss PML
nsv469619 Chr.15:73999518 - 74173980 on Build GRCh38 Loss GOLGA6A LOC732265 PML ISLR2 ISLR LOC283731
nsv833052 Chr.15:73958037 - 74084809 on Build GRCh38 Gain+Loss GOLGA6A PML STOML1
nsv509575 Chr.15:74018397 - 74102404 on Build GRCh38 Insertion GOLGA6A LOC732265 PML
nsv518316 Chr.15:73998652 - 74038742 on Build GRCh38 Gain PML
esv2760040 Chr.15:73922773 - 74172575 on Build GRCh38 Gain+Loss GOLGA6A LOC732265 PML ISLR2 LOXL1 LOC283731 STOML1 LOXL1-AS1
nsv1121512 Chr.15:72670085 - 75273877 on Build GRCh38 Deletion LOC101929333 LOC102723750 ULK3 TBC1D21 SCAMP5 PPCDC CYP1A2 ARID3B LOC283731 LOXL1-AS1 CYP11A1 HCN4 REC114 LOC107984728 MIR6881 ISLR UBL7 NPTN-IT1 EDC3 MPI LOC729739 UBL7-AS1 STRA6 CSK CD276 LMAN1L C15orf59-AS1 ADPGK-AS1 HIGD2B ISLR2 LOC105376731 NEO1 BBS4 ADPGK SEMA7A C15orf39 LOC732265 SCAMP2 CCDC33 GOLGA6C RPP25 MIR6882 CPLX3 CYP1A1 STOML1 NPTN GOLGA6A MIR4513 LOXL1 COX5A CLK3 C15orf59 PML FAM219B

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More Information


Additional Information:

For this assay, SNP(s) [rs117524612] 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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