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

Chr.9:133065057 on build GRCh38
Cytoband
9q34.13
Assay ID Hs02191002_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 1056

Gene Name:

 carboxyl ester lipase

Gene Aliases:

 BAL, BSDL, BSSL, CELL, CEase, FAP, FAPP, LIPA, MODY8

Location:

 Chr.9:133061978-133071863 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 3 - Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CEL NM_001807.4 NP_001798.2
AF081673.1 AAC71012.1
AK299965.1
BC042510.1 AAH42510.1
M85201.1 AAA52014.1
S79774.1 AAB35488.2
X54457.1 CAA38325.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2739138 Chr.9:132727483 - 135521553 on Build GRCh38 Deletion LOC101448202 LCN1 TMEM8C LOC105376306 CELP ABO LOC100130548 GFI1B MIR3689C VAV2 RXRA LOC101928193 AK8 MIR3689D1 STKLD1 SARDH LOC101928525 OLFM1 LINC00094 SLC2A6 REXO4 MIR3689B CACFD1 SNORD36B PPP1R26-AS1 PPP1R26 ADAMTS13 LOC401557 SURF2 SNORD36A DBH-AS1 SURF6 WDR5 GTF3C5 MIR3689D2 COL5A1-AS1 DBH RPL7A OBP2B MIR3689A SNORD24 SNORD36C RALGDS GBGT1 MRPS2 MIR4669 MIR3689E SPACA9 RNU6ATAC SURF1 MED22 ADAMTSL2 MIR6877 MIR3689F MIR548AW LOC100996574 C9orf62 CEL C9orf116 FCN1 COL5A1 BRD3 TSC1 SURF4 FAM163B FCN2 SNORD141A
nsv1161913 Chr.9:133059798 - 133090275 on Build GRCh38 Duplication LOC100996574 CEL CELP
nsv466606 Chr.9:133030314 - 133080285 on Build GRCh38 Loss MIR6877 LOC100996574 LOC105376306 CEL GTF3C5
nsv6746 Chr.9:133044293 - 133068877 on Build GRCh38 Insertion MIR6877 LOC100996574 CEL GTF3C5
nsv951795 Chr.9:133060014 - 133070813 on Build GRCh38 Deletion LOC100996574 CEL
esv3621932 Chr.9:133063192 - 133080639 on Build GRCh38 Gain CEL
dgv12925n54 Chr.9:133061291 - 133082065 on Build GRCh38 Gain LOC100996574 CEL
nsv819112 Chr.9:133058467 - 133082220 on Build GRCh38 Gain LOC100996574 CEL GTF3C5
esv2764128 Chr.9:133061625 - 133082053 on Build GRCh38 Gain+Loss CEL
nsv831744 Chr.9:132980050 - 133174043 on Build GRCh38 Gain+Loss MIR6877 LOC100996574 LOC105376306 CEL RALGDS GTF3C5 CELP GBGT1 GFI1B SNORD141A
esv3573407 Chr.9:133061226 - 133081633 on Build GRCh38 Loss LOC100996574 CEL
nsv508564 Chr.9:133013830 - 133073076 on Build GRCh38 Deletion MIR6877 LOC100996574 LOC105376306 CEL GTF3C5 SNORD141A
esv2761264 Chr.9:133054342 - 133082053 on Build GRCh38 Loss LOC100996574 CEL GTF3C5
nsv825135 Chr.9:133061315 - 133073868 on Build GRCh38 Gain LOC100996574 CEL
nsv825138 Chr.9:133063968 - 133081502 on Build GRCh38 Loss CEL
esv3576709 Chr.9:133060063 - 133092673 on Build GRCh38 Gain LOC100996574 CEL CELP

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More Information


Additional Information:

For this assay, SNP(s) [rs113056079] 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 Non-exonic DGV Variation

Panther Classification:

Molecular Function -

cell adhesion molecule

Gene Ontology Categories:

Function(s) Process(es)


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