Genomic Map
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Target Gene Details
Entrez Gene ID: | 5338 |
Gene Name: | phospholipase D2 |
Gene Aliases: |
- |
Location: |
Chr.17:4807101-4823432 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PLD2 | NM_001243108.1 | 13 | 1351 | NP_001230037.1 |
| NM_002663.4 | 13 | 1351 | NP_002654.3 | |
| XM_005256696.2 | 4 | 411 | XP_005256753.1 | |
| XM_017024764.1 | 13 | 1351 | XP_016880253.1 | |
| AB209374.1 | 10 | 1954 | BAD92611.1 | |
| AF033850.1 | 13 | 1386 | AAD04197.1 | |
| AF035483.1 | 12 | 1225 | AAC24498.1 | |
| AF038440.1 | 13 | 1309 | AAB96655.1 | |
| AF038441.1 | 13 | 1309 | AAB96656.1 | |
| AK304246.1 | 13 | 1304 | ||
| AK314797.1 | 13 | 1269 | ||
| AY178289.1 | 4 | 316 | AAO21120.1 | |
| BC015033.1 | 13 | 1312 | AAH15033.1 | |
| BC056871.1 | 13 | 1260 | AAH56871.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833347 | Chr.17:4785297 - 4955981 on Build GRCh38 | Loss |
 GLTPD2
RNF167
SLC25A11
GP1BA
PSMB6
PFN1
ENO3
MINK1
LOC107984973
C17orf107
PLD2
VMO1
CHRNE
|
| esv3639795 | Chr.17:4812578 - 4820832 on Build GRCh38 | Loss |
PLD2
|
| nsv574273 | Chr.17:4585589 - 5460332 on Build GRCh38 | Gain |
DHX33
NUP88
LOC101559451
SPAG7
ZFP3
LOC101928000
PSMB6
ZNF232
PFN1
C1QBP
LOC102724009
ARRB2
SCIMP
SMTNL2
MINK1
C17orf107
ZNF594
MIR6865
VMO1
CHRNE
GLTPD2
RNF167
SLC25A11
LOC400568
KIF1C
LOC100130950
INCA1
ZMYND15
PELP1
GP1BA
SLC52A1
CAMTA2
MED11
ALOX15
CXCL16
ENO3
RABEP1
RPAIN
TM4SF5
LOC107984973
PLD2
USP6
LOC101927979
MIR6864
|
| nsv833346 | Chr.17:4646256 - 4860871 on Build GRCh38 | Loss |
GLTPD2
LOC101559451
ZMYND15
PELP1
PSMB6
MED11
CXCL16
ARRB2
MINK1
TM4SF5
LOC107984973
PLD2
VMO1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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