Hs03923870_cn

• Gene Symbol: SEC14L5
• Assay Reference Genome Location: Chr.16:4973416 on build GRCh38
• Cytoband: 16p13.3

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
esv3892763	Chr.16:4971982 - 4977763 on Build GRCh38	Loss	SEC14L5
esv2750431	Chr.16:4973232 - 4973625 on Build GRCh38	Deletion	SEC14L5
nsv1042612	Chr.16:4965694 - 5150514 on Build GRCh38	Loss	C16orf89 NAGPA EEF2KMT NAGPA-AS1 SEC14L5 ALG1
nsv528586	Chr.16:4951303 - 5021669 on Build GRCh38	Gain	SEC14L5
esv3892762	Chr.16:4967386 - 5060625 on Build GRCh38	Gain	C16orf89 NAGPA NAGPA-AS1 SEC14L5
esv3637714	Chr.16:4958035 - 5079276 on Build GRCh38	Gain	C16orf89 NAGPA NAGPA-AS1 SEC14L5 ALG1
esv3637713	Chr.16:4957958 - 5307305 on Build GRCh38	Gain	C16orf89 NAGPA EEF2KMT NAGPA-AS1 SEC14L5 RBFOX1 ALG1
esv25186	Chr.16:4858500 - 5142800 on Build GRCh38	Gain	C16orf89 NAGPA UBN1 EEF2KMT NAGPA-AS1 SEC14L5 PPL ALG1
esv2761893	Chr.16:4941276 - 4995458 on Build GRCh38	Loss	SEC14L5
esv2422516	Chr.16:4775920 - 5160979 on Build GRCh38	Deletion	C16orf89 NAGPA UBN1 EEF2KMT NAGPA-AS1 GLYR1 SMIM22 SEC14L5 PPL SEPT12 ALG1 ROGDI
nsv1046986	Chr.16:4049000 - 5555721 on Build GRCh38	Gain	C16orf89 UBN1 EEF2KMT MGRN1 SEC14L5 SRL HMOX2 SEPT12 NAGPA CORO7 C16orf71 ADCY9 NMRAL1 TFAP4 ROGDI NAGPA-AS1 GLYR1 SMIM22 CDIP1 GLIS2-AS1 ANKS3 ZNF500 GLIS2 LOC105371063 LINC01569 NUDT16L1 DNAJA3 PAM16 RBFOX1 PPL CORO7-PAM16 VASN MIR6769A ALG1 C16orf96 UBALD1
esv2750432	Chr.16:4973314 - 4973510 on Build GRCh38	Deletion	SEC14L5
nsv457360	Chr.16:4960912 - 5284683 on Build GRCh38	Loss	C16orf89 NAGPA EEF2KMT NAGPA-AS1 SEC14L5 RBFOX1 ALG1
esv2760069	Chr.16:4922849 - 5374828 on Build GRCh38	Gain+Loss	C16orf89 NAGPA EEF2KMT NAGPA-AS1 SEC14L5 RBFOX1 PPL ALG1

More Information

Additional Information:

For this assay, SNP(s) [rs150801469] 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:

Process(es)

transport

Function(s)

transporter activity