Genomic Map
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Target Gene Details
Entrez Gene ID: | 4605 |
Gene Name: | MYB proto-oncogene like 2 |
Gene Aliases: |
B-MYB, BMYB |
Location: |
Chr.20:43667019-43716496 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MYBL2 | NM_001278610.1 | NP_001265539.1 | ||
| NM_002466.3 | NP_002457.1 | |||
| BC007585.1 | AAH07585.1 | |||
| DC395847.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1057847 | Chr.20:42652464 - 44431352 on Build GRCh38 | Loss |
 TOX2
LOC101927138
R3HDML
GDAP1L1
LOC101927200
FITM2
GTSF1L
L3MBTL1
IFT52
OSER1
PTPRT
SRSF6
JPH2
OSER1-AS1
MYBL2
HNF4A-AS1
LOC105372626
LOC101927159
MIR3646
SGK2
HNF4A
|
| esv3645886 | Chr.20:43653014 - 43756886 on Build GRCh38 | Gain |
MYBL2
LOC101927200
GTSF1L
|
| nsv3385 | Chr.20:43641073 - 43676907 on Build GRCh38 | Deletion |
IFT52
MYBL2
|
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Additional Information:
For this assay, SNP(s) [rs527976577,rs549305850] 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
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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