Genomic Map
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Target Gene Details
Entrez Gene ID: | 94120 |
Gene Name: | synaptotagmin like 3 |
Gene Aliases: |
SLP3 |
Location: |
Chr.6:158644881-158766298 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SYTL3 | NM_001009991.3 | NP_001009991.2 | ||
| NM_001242384.1 | NP_001229313.1 | |||
| NM_001242394.1 | NP_001229323.1 | |||
| NM_001242395.1 | NP_001229324.1 | |||
| XM_005267215.4 | XP_005267272.1 | |||
| XM_005267218.4 | XP_005267275.1 | |||
| XM_006715605.3 | XP_006715668.1 | |||
| XM_006715606.3 | XP_006715669.1 | |||
| XM_006715611.3 | XP_006715674.1 | |||
| XM_011536254.2 | XP_011534556.1 | |||
| XM_017011495.1 | XP_016866984.1 | |||
| XM_017011496.1 | XP_016866985.1 | |||
| XM_017011497.1 | XP_016866986.1 | |||
| XM_017011498.1 | XP_016866987.1 | |||
| XM_017011499.1 | XP_016866988.1 | |||
| AK092729.1 | ||||
| AK131092.1 | BAC85142.1 | |||
| AK298712.1 | ||||
| BC085612.1 | AAH85612.1 | |||
| DB175440.1 | ||||
| DC394549.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv949875 | Chr.6:158652469 - 158655868 on Build GRCh38 | Duplication |
 SYTL3
|
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Additional Information:
For this assay, SNP(s) [rs112459129,rs73797071] 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
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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