Genomic Map
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Target Gene Details
Entrez Gene ID: | 84515 |
Gene Name: | minichromosome maintenance 8 homologous recombination repair factor |
Gene Aliases: |
C20orf154, POF10, dJ967N21.5 |
Location: |
Chr.20:5950652-6000941 on Build GRCh38 |
Assay Gene Location: | Within Intron 18 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MCM8 | NM_001281520.1 | NP_001268449.1 | ||
| NM_001281521.1 | NP_001268450.1 | |||
| NM_001281522.1 | NP_001268451.1 | |||
| NM_032485.5 | NP_115874.3 | |||
| NM_182802.2 | NP_877954.1 | |||
| XM_017028105.1 | XP_016883594.1 | |||
| XM_017028106.1 | XP_016883595.1 | |||
| XM_017028107.1 | XP_016883596.1 | |||
| AJ439063.1 | CAD27750.1 | |||
| AK027644.1 | BAB55260.1 | |||
| AK297806.1 | ||||
| AK314654.1 | ||||
| AY158211.1 | AAO21222.1 | |||
| BC008830.2 | AAH08830.2 | |||
| BC080656.1 | AAH80656.1 | |||
| BC101054.1 | AAI01055.1 | |||
| BC101055.1 | AAI01056.1 | |||
| BC101056.1 | AAI01057.1 | |||
| BC101057.1 | AAI01058.1 | |||
| KU178803.1 | ||||
| KU178804.1 | ||||
| KU178805.1 |
Target Gene Details
Entrez Gene ID: | 101929225 |
Gene Name: | MCM8 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.20:5990795-6005821 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MCM8-AS1 | NR_110101.1 | |||
| AK058185.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3575356 | Chr.20:5954200 - 6068502 on Build GRCh38 | Gain |
 LRRN4
MCM8
CRLS1
MCM8-AS1
|
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Additional Information:
For this assay, SNP(s) [rs79983509] 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
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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