Assay Details
Target Gene Details
Entrez Gene ID: | 79906 |
Gene Name: | MORN repeat containing 1 |
Gene Aliases: |
- |
Location: |
Chr.1:2321253-2391751 on Build GRCh38 |
Assay Gene Location: | Within Intron 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MORN1 | NM_024848.2 | NP_079124.1 | ||
| XM_005244798.2 | XP_005244855.1 | |||
| XM_011542169.1 | XP_011540471.1 | |||
| XM_011542170.2 | XP_011540472.1 | |||
| XM_011542172.2 | XP_011540474.1 | |||
| XM_011542173.2 | XP_011540475.1 | |||
| XM_011542174.2 | XP_011540476.1 | |||
| XM_011542176.1 | XP_011540478.1 | |||
| AK024003.1 | BAB14768.1 | |||
| AK310323.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv951557 | Chr.1:2266062 - 2564661 on Build GRCh38 | Deletion |
|
| nsv834668 | Chr.1:2224327 - 2392938 on Build GRCh38 | Loss |
|
| nsv482937 | Chr.1:10001 - 2368561 on Build GRCh38 | Loss |
|
| nsv470682 | Chr.1:2188394 - 2378754 on Build GRCh38 | Loss |
|
| nsv4742 | Chr.1:2304725 - 2350763 on Build GRCh38 | Insertion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115687241,rs116190040] 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