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See other SEC14L5 CNV Assays ›
Gene Symbol
SEC14L5
Assay Reference Genome
Location

Chr.16:4975918 on build GRCh38
Cytoband
16p13.3
Assay ID Hs03949044_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 9717

Gene Name:

 SEC14 like lipid binding 5

Gene Aliases:

 PRELID4B

Location:

 Chr.16:4958317-5019155 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SEC14L5 NM_014692.1 NP_055507.1
AB007880.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3637714 Chr.16:4958035 - 5079276 on Build GRCh38 Gain NAGPA-AS1 SEC14L5 C16orf89 NAGPA ALG1
esv3637713 Chr.16:4957958 - 5307305 on Build GRCh38 Gain NAGPA-AS1 SEC14L5 C16orf89 EEF2KMT NAGPA RBFOX1 ALG1
esv25186 Chr.16:4858500 - 5142800 on Build GRCh38 Gain NAGPA-AS1 SEC14L5 PPL C16orf89 UBN1 EEF2KMT NAGPA ALG1
esv2761893 Chr.16:4941276 - 4995458 on Build GRCh38 Loss SEC14L5
esv3892763 Chr.16:4971982 - 4977763 on Build GRCh38 Loss SEC14L5
esv2422516 Chr.16:4775920 - 5160979 on Build GRCh38 Deletion NAGPA-AS1 SMIM22 SEC14L5 PPL C16orf89 UBN1 SEPT12 EEF2KMT ROGDI GLYR1 NAGPA ALG1
nsv1046986 Chr.16:4049000 - 5555721 on Build GRCh38 Gain GLIS2-AS1 C16orf96 PPL UBN1 CDIP1 LINC01569 ZNF500 DNAJA3 SMIM22 EEF2KMT NUDT16L1 NAGPA MIR6769A HMOX2 MGRN1 NAGPA-AS1 C16orf71 SRL SEPT12 CORO7 LOC105371063 ALG1 UBALD1 CORO7-PAM16 NMRAL1 GLIS2 SEC14L5 C16orf89 VASN TFAP4 ROGDI ANKS3 GLYR1 PAM16 RBFOX1 ADCY9
nsv1042612 Chr.16:4965694 - 5150514 on Build GRCh38 Loss NAGPA-AS1 SEC14L5 C16orf89 EEF2KMT NAGPA ALG1
nsv457360 Chr.16:4960912 - 5284683 on Build GRCh38 Loss NAGPA-AS1 SEC14L5 C16orf89 EEF2KMT NAGPA RBFOX1 ALG1
nsv528586 Chr.16:4951303 - 5021669 on Build GRCh38 Gain SEC14L5
esv2760069 Chr.16:4922849 - 5374828 on Build GRCh38 Gain+Loss NAGPA-AS1 SEC14L5 PPL C16orf89 EEF2KMT NAGPA RBFOX1 ALG1
esv3892762 Chr.16:4967386 - 5060625 on Build GRCh38 Gain NAGPA-AS1 SEC14L5 C16orf89 NAGPA

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More Information


Additional Information:

For this assay, SNP(s) [rs73527335] 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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