Genomic Map
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Target Gene Details
Entrez Gene ID: | 7048 |
Gene Name: | transforming growth factor beta receptor 2 |
Gene Aliases: |
AAT3, FAA3, LDS1B, LDS2, LDS2B, MFS2, RIIC, TAAD2, TGFR-2, TGFbeta-RII |
Location: |
Chr.3:30606490-30694142 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TGFBR2 | NM_001024847.2 | NP_001020018.1 | ||
| NM_003242.5 | NP_003233.4 | |||
| XM_011534043.2 | XP_011532345.1 | |||
| XM_011534045.2 | XP_011532347.1 | |||
| XM_017007106.1 | XP_016862595.1 | |||
| AK300383.1 | ||||
| AK304404.1 | ||||
| AK314102.1 | ||||
| AL554950.3 | ||||
| CB988859.1 | ||||
| D28131.1 | BAA05673.1 | |||
| DB493906.1 | ||||
| KC792576.1 | ||||
| KC792577.1 | ||||
| KC792578.1 | ||||
| KC792579.1 | ||||
| KC792580.1 | ||||
| KU178359.1 | ||||
| KU178360.1 | ||||
| M85079.1 | AAA61164.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv954457 | Chr.3:30629909 - 30647408 on Build GRCh38 | Duplication |
 TGFBR2
|
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Additional Information:
For this assay, SNP(s) [rs76016701] 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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