Genomic Map
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Target Gene Details
Entrez Gene ID: | 23086 |
Gene Name: | exophilin 5 |
Gene Aliases: |
SLAC2-B, SLAC2B |
Location: |
Chr.11:108505431-108607514 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EXPH5 | NM_001144763.1 | 6 | 1479 | NP_001138235.1 |
| NM_001144764.1 | 4 | 1214 | NP_001138236.1 | |
| NM_001144765.1 | 3 | 1165 | NP_001138237.1 | |
| NM_001308019.1 | 7 | 1396 | NP_001294948.1 | |
| NM_015065.2 | 6 | 1523 | NP_055880.2 | |
| XM_011542696.2 | 7 | 1417 | XP_011540998.1 | |
| XM_011542698.2 | 6 | 1863 | XP_011541000.1 | |
| XM_011542700.2 | 6 | 2763 | XP_011541002.1 | |
| XM_017017397.1 | 7 | 1412 | XP_016872886.1 | |
| XM_017017398.1 | 7 | 1409 | XP_016872887.1 | |
| XM_017017399.1 | 6 | 1315 | XP_016872888.1 | |
| XM_017017400.1 | 7 | 2831 | XP_016872889.1 | |
| XM_017017401.1 | 6 | 2760 | XP_016872890.1 | |
| XM_017017402.1 | 7 | 2871 | XP_016872891.1 | |
| XM_017017403.1 | 4 | 2017 | XP_016872892.1 | |
| XM_017017404.1 | 5 | 2714 | XP_016872893.1 | |
| AB014524.1 | 7 | 1396 | ||
| AK303993.1 | 4 | 1194 | ||
| AK304212.1 | 3 | 1166 | ||
| AY099469.1 | 6 | 1509 | AAM44402.1 | |
| BC113119.1 | 6 | 1494 | AAI13120.1 | |
| BC117701.1 | 6 | 1494 | ||
| CR627226.1 | 6 | 1485 | CAH10364.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3627677 | Chr.11:108432125 - 108587091 on Build GRCh38 | Loss |
 KDELC2
C11orf65
EXPH5
|
| esv3627680 | Chr.11:108509006 - 108580807 on Build GRCh38 | Gain |
EXPH5
|
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Additional Information:
For this assay, SNP(s) [rs116565594] 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
|
Gene Ontology Categories:
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