Assay Details
Target Gene Details
Entrez Gene ID: | 80128 |
Gene Name: | tripartite motif containing 46 |
Gene Aliases: |
GENEY, TRIFIC |
Location: |
Chr.1:155173714-155184971 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 14 - Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TRIM46 | NM_001256599.1 | NP_001243528.1 | ||
| NM_001256600.1 | NP_001243529.1 | |||
| NM_001256601.1 | NP_001243530.1 | |||
| NM_001282378.1 | NP_001269307.1 | |||
| NM_025058.4 | NP_079334.3 | |||
| NR_046327.1 | ||||
| NR_046329.1 | ||||
| XM_011510002.1 | XP_011508304.1 | |||
| XM_017002393.1 | XP_016857882.1 | |||
| AK090504.1 | 2 | 708 | ||
| AK096158.1 | ||||
| AK128139.1 | BAC87293.1 | |||
| AK296300.1 | ||||
| AK297318.1 | ||||
| AK309699.1 | ||||
| AY251386.1 | AAP51206.1 | |||
| BC126372.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv527682 | Chr.1:155177242 - 155227671 on Build GRCh38 | Gain |
|
| nsv470741 | Chr.1:155142784 - 155260340 on Build GRCh38 | Loss |
|
| nsv8447 | Chr.1:155172153 - 155184461 on Build GRCh38 | Gain |
|
| nsv1010146 | Chr.1:155146620 - 155231273 on Build GRCh38 | Gain |
|
| nsv2988 | Chr.1:155182130 - 155219701 on Build GRCh38 | Insertion |
|
| nsv547961 | Chr.1:155109822 - 155225189 on Build GRCh38 | Loss |
|
| dgv3n68 | Chr.1:155122502 - 155343618 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114809126] 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