Genomic Map
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Target Gene Details
Entrez Gene ID: | 4207 |
Gene Name: | BORCS8-MEF2B readthrough |
Gene Aliases: |
LOC729991-MEF2B, MEF2B, MEF2BNB-MEF2B |
Location: |
Chr.19:19145567-19192591 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 6 - Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BORCS8-MEF2B | NM_005919.3 | NP_005910.1 | ||
| NR_027307.1 | ||||
| NR_027308.1 | ||||
| AK301086.1 | ||||
| AK316328.1 | ||||
| BC126245.1 | ||||
| BC136457.1 | ||||
| BC171767.1 | ||||
| X63380.1 | CAA44978.1 | |||
| X68502.1 | CAA48515.1 |
Target Gene Details
Entrez Gene ID: | 100271849 |
Gene Name: | myocyte enhancer factor 2B |
Gene Aliases: |
RSRFR2 |
Location: |
Chr.19:19145567-19170289 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MEF2B | NM_001145785.1 | NP_001139257.1 | ||
| AK057210.1 | ||||
| DA488022.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833779 | Chr.19:19052683 - 19202282 on Build GRCh38 | Loss |
 NR2C2AP
RFXANK
BORCS8-MEF2B
BORCS8
MEF2B
ARMC6
SLC25A42
TMEM161A
|
| nsv1151217 | Chr.19:18627369 - 19284914 on Build GRCh38 | Deletion |
COMP
RFXANK
SUGP2
NCAN
BORCS8-MEF2B
BORCS8
DDX49
SLC25A42
TMEM161A
LOC102724360
HOMER3
NR2C2AP
HAPLN4
CRTC1
UPF1
CERS1
TM6SF2
KLHL26
COPE
SUGP1
GDF1
MEF2B
ARMC6
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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