Genomic Map
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Target Gene Details
Entrez Gene ID: | 54869 |
Gene Name: | EPS8 like 1 |
Gene Aliases: |
DRC3, EPS8R1, PP10566 |
Location: |
Chr.19:55075853-55087923 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EPS8L1 | NM_133180.2 | NP_573441.2 | ||
| XM_005259020.1 | XP_005259077.1 | |||
| XM_011527051.2 | XP_011525353.1 | |||
| XM_011527052.2 | XP_011525354.1 | |||
| AF370395.1 | AAQ15231.1 | |||
| AK075098.1 | BAC11399.1 | |||
| AK296732.1 | ||||
| AK309305.1 | ||||
| AK309908.1 | ||||
| AY074928.1 | AAL76117.1 | |||
| BC004907.2 | AAH04907.2 | |||
| DA452167.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv817874 | Chr.19:55067334 - 55103555 on Build GRCh38 | Loss |
 RDH13
EPS8L1
PPP1R12C
|
| esv3644829 | Chr.19:55030893 - 55138732 on Build GRCh38 | Gain |
MIR7975
RDH13
EPS8L1
PPP1R12C
GP6
TNNT1
|
| esv2667609 | Chr.19:54472514 - 55094226 on Build GRCh38 | Deletion |
RDH13
NLRP2
KIR3DL1
KIR2DL4
LOC101928804
MIR8061
LOC102724300
LILRB1
CDC42EP5
GP6
KIR2DS4
LILRP2
LILRB4
FCAR
KIR2DL1
NLRP7
KIR3DL3
PPP1R12C
NCR1
LILRA1
KIR2DL3
KIR3DL2
LILRA2
EPS8L1
KIR3DX1
LAIR2
|
| esv2758772 | Chr.19:55026094 - 55139319 on Build GRCh38 | Gain |
MIR7975
RDH13
EPS8L1
PPP1R12C
GP6
TNNT1
|
| nsv817875 | Chr.19:55070143 - 55090747 on Build GRCh38 | Loss |
EPS8L1
|
| esv2718872 | Chr.19:54472594 - 55094247 on Build GRCh38 | Deletion |
RDH13
NLRP2
KIR3DL1
KIR2DL4
LOC101928804
MIR8061
LOC102724300
LILRB1
CDC42EP5
GP6
KIR2DS4
LILRP2
LILRB4
FCAR
KIR2DL1
NLRP7
KIR3DL3
PPP1R12C
NCR1
LILRA1
KIR2DL3
KIR3DL2
LILRA2
EPS8L1
KIR3DX1
LAIR2
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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