Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 255394 |
Gene Name: | t-complex 11 like 2 |
Gene Aliases: |
- |
Location: |
Chr.12:106302026-106347455 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TCP11L2 | NM_001286262.1 | 1 | 95 | NP_001273191.1 |
| NM_152772.2 | 1 | 95 | NP_689985.1 | |
| XM_005268767.4 | 1 | 106 | XP_005268824.1 | |
| XM_011538131.2 | 1 | 106 | XP_011536433.1 | |
| XM_011538132.2 | 1 | 130 | XP_011536434.1 | |
| XM_017019129.1 | 1 | 107 | XP_016874618.1 | |
| XM_017019130.1 | 1 | 107 | XP_016874619.1 | |
| XM_017019131.1 | XP_016874620.1 | |||
| XM_017019132.1 | 1 | 106 | XP_016874621.1 | |
| XM_017019133.1 | 1 | 107 | XP_016874622.1 | |
| AF306671.1 | 1 | 68 | ||
| AF306673.1 | ||||
| AF306858.1 | 1 | 68 | ||
| AK314055.1 | ||||
| BC033617.1 | 1 | 83 | AAH33617.1 |
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs77370280] 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
Exonic
non-DGV Variation
|
Panther Classification:
Back To Top