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See other CYP2C18 CNV Assays ›
Gene Symbol
CYP2C18
Assay Reference Genome
Location

Chr.10:94694659 on build GRCh38
Cytoband
10q23.33
Assay ID Hs05164104_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 1562

Gene Name:

 cytochrome P450 family 2 subfamily C member 18

Gene Aliases:

 CPCI, CYP2C, CYP2C17, P450-6B/29C, P450IIC17

Location:

 Chr.10:94683494-94736190 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CYP2C18 NM_000772.2 NP_000763.1
NM_001128925.1 NP_001122397.1
AK223510.1 BAD97230.1
AK308558.1
AK313403.1
BC069666.1 AAH69666.1
BC096257.1 AAH96257.1
BC096258.1 AAH96258.1
BC096260.1 AAH96260.1
BX538127.1 CAD98029.1
M61853.1
M61856.1 AAB59356.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1046308 Chr.10:94681543 - 94873255 on Build GRCh38 Loss CYP2C19 CYP2C18
esv2672446 Chr.10:94643689 - 94761824 on Build GRCh38 Deletion CYP2C18
esv3891886 Chr.10:94694399 - 94965778 on Build GRCh38 Loss CYP2C19 CYP2C18 CYP2C9
dgv1355n54 Chr.10:94684492 - 94930614 on Build GRCh38 Loss CYP2C19 CYP2C18 CYP2C9
dgv955n100 Chr.10:94645539 - 94757047 on Build GRCh38 Loss CYP2C18
nsv522538 Chr.10:94645572 - 94787706 on Build GRCh38 Loss CYP2C19 CYP2C18
esv2739707 Chr.10:94680312 - 94940071 on Build GRCh38 Deletion CYP2C19 CYP2C18 CYP2C9
esv3624253 Chr.10:94643661 - 94761810 on Build GRCh38 Loss CYP2C18
dgv956n100 Chr.10:94657052 - 94726747 on Build GRCh38 Loss CYP2C18
esv2657299 Chr.10:94690484 - 94699101 on Build GRCh38 Deletion CYP2C18
esv3624254 Chr.10:94644907 - 94724573 on Build GRCh38 Loss CYP2C18

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More Information


Additional Information:

For this assay, SNP(s) [rs79053633] 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

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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