Assay Details
Target Gene Details
Entrez Gene ID: | 83723 |
Gene Name: | family with sequence similarity 57 member B |
Gene Aliases: |
FP1188 |
Location: |
Chr.16:30024423-30053026 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 8 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM57B | NM_031478.5 | NP_113666.2 | ||
| XM_005255613.3 | XP_005255670.1 | |||
| XM_005255614.3 | XP_005255671.1 | |||
| XM_005255615.2 | XP_005255672.1 | |||
| XM_017023749.1 | XP_016879238.1 | |||
| XM_017023750.1 | XP_016879239.1 | |||
| XM_017023751.1 | XP_016879240.1 | |||
| XM_017023752.1 | XP_016879241.1 | |||
| XM_017023753.1 | XP_016879242.1 | |||
| XM_017023754.1 | XP_016879243.1 | |||
| AB593089.1 | ||||
| AB593090.1 | ||||
| AF370365.1 | AAQ15201.1 | |||
| AL535138.3 | ||||
| BC007892.2 | ||||
| BQ185065.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1160384 | Chr.16:30023148 - 30178660 on Build GRCh38 | Duplication |
|
More Information
Additional Information:
For this assay, SNP(s) [rs201991450] 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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Genomic Map