Assay Details
Target Gene Details
Entrez Gene ID: | 139221 |
Gene Name: | MUM1 like 1 |
Gene Aliases: |
- |
Location: |
Chr.X:106168278-106208961 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MUM1L1 | NM_001171020.1 | NP_001164491.1 | ||
| NM_152423.4 | NP_689636.3 | |||
| XM_005262077.2 | XP_005262134.1 | |||
| XM_011530856.1 | XP_011529158.1 | |||
| XM_011530857.1 | XP_011529159.1 | |||
| XM_017029269.1 | XP_016884758.1 | |||
| AK056478.1 | BAB71194.1 | |||
| BC031229.1 | AAH31229.1 | |||
| CN369699.1 | ||||
| DA720504.1 | ||||
| DB445635.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2752312 | Chr.X:105705935 - 107123872 on Build GRCh38 | Gain |
|
| nsv521259 | Chr.X:105935140 - 106434204 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs147249197] 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