Genomic Map
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Target Gene Details
Entrez Gene ID: | 9723 |
Gene Name: | semaphorin 3E |
Gene Aliases: |
M-SEMAH, M-SemaK, SEMAH, coll-5 |
Location: |
Chr.7:83363906-83649163 on Build GRCh38 |
Assay Gene Location: | Within Exon 18 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SEMA3E | NM_001178129.1 | 17 | 4790 | NP_001171600.1 |
| NM_012431.2 | 17 | 5426 | NP_036563.1 | |
| AB002329.1 | 17 | 5271 | ||
| BC140706.1 | 17 | 4961 | ||
| BC144338.1 | 17 | 4961 | ||
| BC152458.1 | 17 | 5283 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1023612 | Chr.7:82592183 - 83790140 on Build GRCh38 | Loss |
 SEMA3E
PCLO
|
| esv3613933 | Chr.7:83362430 - 83451993 on Build GRCh38 | Loss |
SEMA3E
|
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Additional Information:
For this assay, SNP(s) [rs144720043] 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: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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