Genomic Map
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Target Gene Details
Entrez Gene ID: | 8600 |
Gene Name: | tumor necrosis factor superfamily member 11 |
Gene Aliases: |
CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B, TRANCE, hRANKL2, sOdf |
Location: |
Chr.13:42562736-42608013 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TNFSF11 | NM_003701.3 | NP_003692.1 | ||
| NM_033012.3 | NP_143026.1 | |||
| XM_011535280.2 | XP_011533582.1 | |||
| XM_017020802.1 | XP_016876291.1 | |||
| XM_017020803.1 | XP_016876292.1 | |||
| AB037599.1 | BAA90488.1 | |||
| AB061227.1 | BAB71768.1 | |||
| AB064268.1 | BAB79693.1 | |||
| AB064269.1 | BAB79694.1 | |||
| AB064270.1 | BAB79695.1 | |||
| AF013171.1 | AAC51762.1 | |||
| AF019047.1 | AAB86811.1 | |||
| AF053712.1 | AAC39731.1 | |||
| BC074823.2 | AAH74823.1 | |||
| BC074890.2 | AAH74890.1 | |||
| BC117286.1 | ||||
| BC117288.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832593 | Chr.13:42571804 - 42735651 on Build GRCh38 | Gain |
 TNFSF11
|
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Additional Information:
For this assay, SNP(s) [rs112582842] 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
|
Gene Ontology Categories:
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