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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 RALGDS PPP1R26-AS1 LINC00094 PPP1R26 COL5A1-AS1 LOC101928193 GBGT1 STKLD1 LOC401557 MIR3689E LOC100130548 MIR4669 CEL MIR548AW C9orf116 SNORD141A MIR3689B RXRA SNORD24 MIR3689C FCN2 SARDH RPL7A SURF6 MED22 FAM163B CACFD1 SURF1 BRD3 LCN1 OBP2B SNORD36A GTF3C5 LOC101928525 MIR3689D1 ADAMTS13 MRPS2 LOC100996574 DBH AK8 SNORD36B TMEM8C ADAMTSL2 TSC1 SLC2A6 MIR3689F SURF2 SNORD36C WDR5 CELP COL5A1 OLFM1 SPACA9 REXO4 ABO MIR6877 C9orf62 LOC105376306 LOC101448202 MIR3689D2 GFI1B DBH-AS1 VAV2 MIR3689A RNU6ATAC SURF4 FCN1
nsv1161913 Chr.9:133059798 - 133090275 on Build GRCh38 Duplication CEL LOC100996574 CELP
nsv6746 Chr.9:133044293 - 133068877 on Build GRCh38 Insertion MIR6877 GTF3C5 CEL LOC100996574
nsv615596 Chr.9:133030314 - 133080285 on Build GRCh38 Loss MIR6877 GTF3C5 LOC105376306 CEL LOC100996574
nsv951795 Chr.9:133060014 - 133070813 on Build GRCh38 Deletion CEL LOC100996574
esv3621931 Chr.9:133063192 - 133080639 on Build GRCh38 Loss CEL
dgv12925n54 Chr.9:133061291 - 133082065 on Build GRCh38 Gain CEL LOC100996574
nsv819112 Chr.9:133058467 - 133082220 on Build GRCh38 Gain GTF3C5 CEL LOC100996574
esv2764128 Chr.9:133061625 - 133082053 on Build GRCh38 Gain+Loss CEL
nsv831744 Chr.9:132980050 - 133174043 on Build GRCh38 Gain+Loss MIR6877 RALGDS GTF3C5 SNORD141A LOC105376306 GFI1B CEL LOC100996574 GBGT1 CELP
esv3573407 Chr.9:133061226 - 133081633 on Build GRCh38 Loss CEL LOC100996574
dgv1242n67 Chr.9:133061315 - 133084032 on Build GRCh38 Gain CEL LOC100996574 CELP
esv2761264 Chr.9:133054342 - 133082053 on Build GRCh38 Loss GTF3C5 CEL LOC100996574
nsv508564 Chr.9:133013830 - 133073076 on Build GRCh38 Deletion MIR6877 GTF3C5 SNORD141A LOC105376306 CEL LOC100996574
nsv825138 Chr.9:133063968 - 133081502 on Build GRCh38 Loss CEL
esv3576709 Chr.9:133060063 - 133092673 on Build GRCh38 Gain CEL LOC100996574 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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