Assay Details
Target Gene Details
Entrez Gene ID: | 54437 |
Gene Name: | semaphorin 5B |
Gene Aliases: |
SEMAG, SemG |
Location: |
Chr.3:122909193-123028605 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 25 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SEMA5B | NM_001031702.3 | NP_001026872.2 | ||
| NM_001256346.1 | NP_001243275.1 | |||
| NM_001256347.1 | NP_001243276.1 | |||
| NM_001256348.1 | NP_001243277.1 | |||
| NR_046079.1 | ||||
| XM_017006638.1 | XP_016862127.1 | |||
| AB040878.1 | ||||
| AK001234.1 | BAA91570.1 | |||
| AY358124.1 | AAQ88491.1 | |||
| BC077726.1 | AAH77726.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv829706 | Chr.3:122797072 - 122951740 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs80353916] 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