Assay Details
Target Gene Details
Entrez Gene ID: | 60487 |
Gene Name: | tRNA methyltransferase 11 homolog |
Gene Aliases: |
C6orf75, MDS024, TRM11, TRMT11-1 |
Location: |
Chr.6:125986430-126083131 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TRMT11 | NM_001031712.2 | NP_001026882.2 | ||
| XM_017011168.1 | XP_016866657.1 | |||
| XM_017011169.1 | XP_016866658.1 | |||
| AF182423.1 | AAG14959.1 | |||
| AF532977.1 | AAQ10284.1 | |||
| AK308651.1 | ||||
| BC056878.1 | AAH56878.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1025069 | Chr.6:125973448 - 126003809 on Build GRCh38 | Loss |
|
| nsv1022677 | Chr.6:125935606 - 126195159 on Build GRCh38 | Gain |
|
| nsv1019490 | Chr.6:125927450 - 126221150 on Build GRCh38 | Loss |
|
| nsv830796 | Chr.6:125844487 - 126015022 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs116438177] 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: |
|

Genomic Map