Genomic Map
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Target Gene Details
Entrez Gene ID: | 7082 |
Gene Name: | tight junction protein 1 |
Gene Aliases: |
ZO-1 |
Location: |
Chr.15:29699367-29968919 on Build GRCh38 |
Assay Gene Location: | Within Exon 30 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TJP1 | NM_001301025.1 | 26 | 4695 | NP_001287954.1 |
| NM_001301026.1 | 25 | 4470 | NP_001287955.1 | |
| NM_003257.4 | 25 | 4931 | NP_003248.3 | |
| NM_175610.3 | 24 | 4691 | NP_783297.2 | |
| XM_005254617.3 | 26 | 4815 | XP_005254674.2 | |
| XM_005254618.3 | 25 | 4562 | XP_005254675.1 | |
| XM_005254619.3 | 25 | 4575 | XP_005254676.2 | |
| XM_005254620.3 | 25 | 4575 | XP_005254677.2 | |
| XM_011521972.2 | 26 | 4815 | XP_011520274.2 | |
| XM_017022521.1 | 27 | 4866 | XP_016878010.1 | |
| XM_017022522.1 | 27 | 4866 | XP_016878011.1 | |
| XM_017022523.1 | 27 | 4866 | XP_016878012.1 | |
| XM_017022524.1 | 26 | 4626 | XP_016878013.1 | |
| XM_017022525.1 | 26 | 4628 | XP_016878014.1 | |
| XM_017022526.1 | 26 | 4613 | XP_016878015.1 | |
| XM_017022527.1 | 26 | 4654 | XP_016878016.1 | |
| XM_017022528.1 | 25 | 4577 | XP_016878017.1 | |
| XM_017022529.1 | 25 | 4562 | XP_016878018.1 | |
| XM_017022530.1 | 24 | 4322 | XP_016878019.1 | |
| XM_017022531.1 | 27 | 4696 | XP_016878020.1 | |
| AB370197.1 | 24 | 4435 | ||
| AK302971.1 | 6 | 1496 | ||
| AK304758.1 | 25 | 4562 | ||
| BC111712.1 | 25 | 4833 | AAI11713.1 | |
| BX640879.1 | 25 | 4471 | CAE45936.1 | |
| CR749235.1 | 17 | 3224 | CAH18091.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1040778 | Chr.15:28689598 - 30515727 on Build GRCh38 | Loss |
 GOLGA8R
LOC100289656
APBA2
LOC105370746
GOLGA8J
LOC105370751
LOC100130111
CHRFAM7A
LOC107984752
PDCD6IPP2
WHAMMP2
LOC101060569
GOLGA8M
GOLGA8T
GOLGA6L7P
ULK4P3
NSMCE3
TJP1
DKFZP434L187
FAM189A1
|
| nsv832945 | Chr.15:29640395 - 29831518 on Build GRCh38 | Gain |
LOC100130111
TJP1
|
| nsv527255 | Chr.15:28754022 - 30074044 on Build GRCh38 | Gain |
LOC100289656
APBA2
PDCD6IPP2
WHAMMP2
LOC100130111
GOLGA6L7P
NSMCE3
TJP1
LOC107984752
FAM189A1
|
| esv2751526 | Chr.15:28724519 - 30687025 on Build GRCh38 | Loss |
GOLGA8R
APBA2
LOC105370751
LOC100130111
CHRFAM7A
LOC107984752
LOC100288637
ULK4P3
TJP1
LOC100289656
LOC100996413
LOC105370746
GOLGA8J
ARHGAP11B
ULK4P2
PDCD6IPP2
LOC101927579
WHAMMP2
LOC101060569
GOLGA8H
GOLGA8T
GOLGA6L7P
NSMCE3
DKFZP434L187
FAM189A1
|
| nsv1039798 | Chr.15:28724126 - 30158154 on Build GRCh38 | Gain |
LOC100289656
APBA2
GOLGA8J
LOC100130111
LOC107984752
PDCD6IPP2
WHAMMP2
GOLGA8T
GOLGA6L7P
ULK4P3
NSMCE3
TJP1
FAM189A1
|
| nsv568675 | Chr.15:29035149 - 29916451 on Build GRCh38 | Gain |
APBA2
LOC100130111
NSMCE3
TJP1
FAM189A1
|
| nsv832944 | Chr.15:29568858 - 29789854 on Build GRCh38 | Gain+Loss |
LOC100130111
TJP1
FAM189A1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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