Assay Details
Target Gene Details
Entrez Gene ID: | 346653 |
Gene Name: | family with sequence similarity 71 member F2 |
Gene Aliases: |
FAM137B |
Location: |
Chr.7:128671628-128702262 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM71F2 | NM_001012454.5 | 1 | 84 | NP_001012457.3 |
NM_001128926.3 | 1 | 84 | NP_001122398.1 | |
NM_001290254.1 | 1 | 66 | NP_001277183.1 | |
NM_001290255.1 | 1 | 84 | NP_001277184.1 | |
XM_011516128.2 | 1 | 66 | XP_011514430.1 | |
XM_011516129.2 | 1 | 66 | XP_011514431.1 | |
XM_011516130.2 | 1 | 66 | XP_011514432.1 | |
XM_011516131.2 | 1 | 66 | XP_011514433.1 | |
XM_011516132.2 | 1 | 66 | XP_011514434.1 | |
XM_011516135.2 | XP_011514437.1 | |||
XM_011516136.2 | XP_011514438.1 | |||
XM_017012147.1 | 1 | 84 | XP_016867636.1 | |
XM_017012149.1 | 1 | 66 | XP_016867638.1 | |
BC047310.1 | 1 | 56 | AAH47310.2 | |
BC066973.1 | 1 | 58 | AAH66973.2 | |
BC105729.1 | 1 | 57 | ||
BC105730.1 | 1 | 57 | ||
BC105731.1 | 1 | 57 | ||
BI828876.1 | 1 | 64 | ||
HY039605.1 | 1 | 85 | ||
HY046252.1 | 1 | 67 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2670312 | Chr.7:128499519 - 128999613 on Build GRCh38 | Deletion |
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esv2735137 | Chr.7:128499440 - 128999664 on Build GRCh38 | Deletion |
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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) [rs74343948] 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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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)