Assay Details
Target Gene Details
Entrez Gene ID: | 51208 |
Gene Name: | claudin 18 |
Gene Aliases: |
SFTA5, SFTPJ |
Location: |
Chr.3:137998816-138033652 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CLDN18 | NM_001002026.2 | NP_001002026.1 | ||
NM_016369.3 | NP_057453.1 | |||
AF221069.1 | AAF26448.1 | |||
AF349452.1 | AAL15637.1 | |||
AK098474.1 | ||||
AK298103.1 | ||||
AY358479.1 | AAQ88843.1 | |||
BC142708.1 | ||||
BC146668.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv428422 | Chr.3:137344347 - 138686784 on Build GRCh38 | Gain+Loss |
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nsv591852 | Chr.3:137964915 - 138022297 on Build GRCh38 | Loss |
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esv2751978 | Chr.3:137996460 - 138171908 on Build GRCh38 | Loss |
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esv2759180 | Chr.3:137892947 - 138214993 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs114302616] 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: |
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Panther Classification:
Gene Ontology Categories:
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