Genomic Map
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Target Gene Details
Entrez Gene ID: | 619343 |
Gene Name: | ERICH1 antisense RNA 1 |
Gene Aliases: |
C8orf68 |
Location: |
Chr.8:737605-1137777 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ERICH1-AS1 | NR_073397.1 | |||
| HY026606.1 |
Target Gene Details
Entrez Gene ID: | 105377777 |
Gene Name: | uncharacterized LOC105377777 |
Gene Aliases: |
- |
Location: |
Chr.8:878741-882930 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC105377777 | XM_011534774.2 | XP_011533076.1 | ||
| XM_011534777.2 | XP_011533079.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1015350 | Chr.8:818461 - 914408 on Build GRCh38 | Loss |
 LOC105377777
ERICH1-AS1
|
| nsv1024325 | Chr.8:651043 - 3203837 on Build GRCh38 | Gain |
ARHGEF10
CLN8
LOC105377774
LOC101927752
DLGAP2-AS1
LOC100131395
ERICH1-AS1
LOC286083
KBTBD11
LOC105377781
DLGAP2
CSMD1
LOC105377777
LOC105377776
LOC101927815
LOC101928058
LOC401442
KBTBD11-OT1
LOC105377792
MIR596
ERICH1
MIR7160
MYOM2
MIR3674
|
| nsv465270 | Chr.8:838912 - 899254 on Build GRCh38 | Loss |
LOC105377777
ERICH1-AS1
|
| esv3615798 | Chr.8:703312 - 881713 on Build GRCh38 | Gain |
LOC105377777
LOC401442
ERICH1
ERICH1-AS1
|
| esv3615801 | Chr.8:804495 - 901794 on Build GRCh38 | Gain |
LOC105377777
ERICH1-AS1
|
| nsv609472 | Chr.8:665117 - 977722 on Build GRCh38 | Gain |
LOC105377777
LOC401442
ERICH1
ERICH1-AS1
|
| esv3572379 | Chr.8:820837 - 899254 on Build GRCh38 | Loss |
LOC105377777
ERICH1-AS1
|
| nsv609452 | Chr.8:240568 - 919170 on Build GRCh38 | Loss |
LOC105377777
LOC401442
FBXO25
TDRP
LOC105377774
FAM87A
ERICH1
ERICH1-AS1
ZNF596
|
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Additional Information:
For this assay, SNP(s) [rs113333358] 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
|
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