Assay Details
Target Gene Details
Entrez Gene ID: | 152189 |
Gene Name: | CKLF like MARVEL transmembrane domain containing 8 |
Gene Aliases: |
CKLFSF8, CKLFSF8-V2 |
Location: |
Chr.3:32238679-32370325 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CMTM8 | NM_001320308.1 | NP_001307237.1 | ||
NM_178868.4 | NP_849199.2 | |||
XM_011533416.2 | XP_011531718.1 | |||
XM_017005779.1 | XP_016861268.1 | |||
AF474370.2 | AAN73034.1 | |||
AY598783.1 | ||||
BC041390.2 | AAH41390.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1003285 | Chr.3:31386933 - 33172886 on Build GRCh38 | Gain |
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nsv590046 | Chr.3:32297503 - 32302814 on Build GRCh38 | Loss |
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esv23045 | Chr.3:32297501 - 32298032 on Build GRCh38 | Loss |
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esv3561699 | Chr.3:32297446 - 32298360 on Build GRCh38 | Deletion |
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esv3595770 | Chr.3:32297309 - 32298230 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) [rs139243578] 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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