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- Gene Symbol
- SELENBP1
- Assay Reference Genome
Location
Chr.1:151368204 on build GRCh38- Cytoband
Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 8991 |
Gene Name: | selenium binding protein 1 |
Gene Aliases: |
EHMTO, HEL-S-134P, LPSB, MTO, SBP56, SP56, hSBP |
Location: |
Chr.1:151364304-151372705 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SELENBP1 | NM_001258288.2 | NP_001245217.1 | ||
| NM_001258289.2 | NP_001245218.1 | |||
| NM_003944.4 | NP_003935.2 | |||
| XM_047433576.1 | XP_047289532.1 | |||
| AK023875.1 | BAB14709.1 | |||
| AK296661.1 | BAG59258.1 | |||
| AK298355.1 | BAG60599.1 | |||
| AK303815.1 | BAG64765.1 | |||
| AK310044.1 | ||||
| AK315643.1 | BAG38010.1 | |||
| BC009084.1 | AAH09084.1 | |||
| BC032997.1 | AAH32997.1 | |||
| CR456852.1 | CAG33133.1 | |||
| EU794660.1 | ACJ13714.1 | |||
| U29091.1 | AAB02395.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv522840 | Chr.1:150961247 - 151375270 on Build GRCh38 | Gain |
 SCNM1
CDC42SE1
TMOD4
TNFAIP8L2
BNIPL
RFX5-AS1
ANXA9
GABPB2
VPS72
LYSMD1
MLLT11
ZNF687-AS1
PRUNE1
PI4KB
PSMD4
C1orf56
SEMA6C
CERS2
ZNF687
MINDY1
RFX5
PIP5K1A
SELENBP1
SETDB1
TNFAIP8L2-SCNM1
|
| dgv53e214 | Chr.1:151359619 - 151441151 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| nsv8380 | Chr.1:151357411 - 151437870 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| nsv831581 | Chr.1:151316675 - 151506129 on Build GRCh38 | Loss |
PSMB4
RFX5
RFX5-AS1
PI4KB
SELENBP1
POGZ
|
| nsv441714 | Chr.1:151364223 - 151425402 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| esv3587526 | Chr.1:151360740 - 151441151 on Build GRCh38 | Loss |
PSMB4
SELENBP1
POGZ
|
| esv2758969 | Chr.1:151356318 - 151439159 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| esv3587525 | Chr.1:151360256 - 151412906 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| nsv824575 | Chr.1:151359057 - 151435620 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| nsv4067263 | Chr.1:151359592 - 151435987 on Build GRCh38 | Duplication |
PSMB4
SELENBP1
POGZ
|
| esv34461 | Chr.1:151268066 - 151439159 on Build GRCh38 | Gain |
PSMB4
ZNF687
RFX5
RFX5-AS1
ZNF687-AS1
PI4KB
SELENBP1
POGZ
|
| nsv1161560 | Chr.1:151359541 - 151436260 on Build GRCh38 | Duplication |
PSMB4
SELENBP1
POGZ
|
| dgv76n145 | Chr.1:151358895 - 151432320 on Build GRCh38 | Duplication |
PSMB4
SELENBP1
POGZ
|
| nsv5981509 | Chr.1:151359872 - 151436237 on Build GRCh38 | Duplication |
PSMB4
SELENBP1
POGZ
|
| esv3894200 | Chr.1:151360691 - 151435217 on Build GRCh38 | Gain |
PSMB4
SELENBP1
POGZ
|
| nsv438026 | Chr.1:151346257 - 151372227 on Build GRCh38 | Loss |
RFX5
RFX5-AS1
SELENBP1
|
| nsv4062004 | Chr.1:151356470 - 151369416 on Build GRCh38 | Duplication |
SELENBP1
|
| nsv6138677 | Chr.1:151359589 - 151436025 on Build GRCh38 | Duplication |
PSMB4
SELENBP1
POGZ
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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