Genomic Map
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Target Gene Details
Entrez Gene ID: | 253738 |
Gene Name: | early B-cell factor 3 |
Gene Aliases: |
COE3, EBF-3, O/E-2, OE-2 |
Location: |
Chr.10:129835232-129964274 on Build GRCh38 |
Assay Gene Location: | Within Exon 19 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EBF3 | NM_001005463.2 | 16 | 2250 | NP_001005463.1 |
| XM_005252667.3 | 17 | 2918 | XP_005252724.1 | |
| XM_005252668.3 | 16 | 2832 | XP_005252725.1 | |
| XM_005252669.3 | 16 | 2805 | XP_005252726.1 | |
| XM_006717739.3 | 17 | 2945 | XP_006717802.1 | |
| XM_006717740.3 | 17 | 2942 | XP_006717803.1 | |
| XM_006717742.3 | 17 | 2837 | XP_006717805.1 | |
| XM_006717743.3 | 16 | 2724 | XP_006717806.1 | |
| XM_006717744.3 | 16 | 2648 | XP_006717807.1 | |
| XM_011539574.2 | 15 | 2660 | XP_011537876.1 | |
| XM_011539575.2 | 12 | 1939 | XP_011537877.1 | |
| XM_017016027.1 | 15 | 2535 | XP_016871516.1 | |
| AK098025.1 | ||||
| AL713797.1 | 1 | 889 | ||
| AL832828.1 | 16 | 2177 | CAH56225.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832023 | Chr.10:129812459 - 130010617 on Build GRCh38 | Gain+Loss |
 MIR4297
EBF3
|
| esv3577850 | Chr.10:128673756 - 129928631 on Build GRCh38 | Gain |
MGMT
MIR4297
EBF3
|
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Additional Information:
For this assay, SNP(s) [rs143792465,rs80280545] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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