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- Gene Symbol
- SELENBP1
- Assay Reference Genome
Location
Chr.1:151365237 on build GRCh38- Cytoband
Genomic Map
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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: | Within Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SELENBP1 | NM_001258288.2 | 9 | 967 | NP_001245217.1 |
| NM_001258289.2 | 10 | 1362 | NP_001245218.1 | |
| NM_003944.4 | 10 | 1153 | NP_003935.2 | |
| XM_047433576.1 | 9 | 1183 | XP_047289532.1 | |
| AK023875.1 | 6 | 2273 | BAB14709.1 | |
| AK296661.1 | 10 | 1360 | BAG59258.1 | |
| AK298355.1 | 10 | 1047 | BAG60599.1 | |
| AK303815.1 | 9 | 962 | BAG64765.1 | |
| AK315643.1 | 10 | 1152 | BAG38010.1 | |
| BC009084.1 | 10 | 1136 | AAH09084.1 | |
| BC032997.1 | 8 | 1567 | AAH32997.1 | |
| BQ045424.1 | 3 | 587 | ||
| CR456852.1 | 9 | 1089 | CAG33133.1 | |
| EU794660.1 | 10 | 1136 | ACJ13714.1 | |
| U29091.1 | 9 | 1093 | 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
PRUNE1
GABPB2
LYSMD1
PI4KB
MLLT11
MINDY1
PSMD4
ZNF687-AS1
TMOD4
SETDB1
C1orf56
RFX5
BNIPL
TNFAIP8L2
TNFAIP8L2-SCNM1
PIP5K1A
SELENBP1
CERS2
CDC42SE1
VPS72
ANXA9
RFX5-AS1
SEMA6C
ZNF687
|
| dgv53e214 | Chr.1:151359619 - 151441151 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| nsv8380 | Chr.1:151357411 - 151437870 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| nsv831581 | Chr.1:151316675 - 151506129 on Build GRCh38 | Loss |
RFX5-AS1
POGZ
RFX5
PI4KB
PSMB4
SELENBP1
|
| nsv441714 | Chr.1:151364223 - 151425402 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| esv3587526 | Chr.1:151360740 - 151441151 on Build GRCh38 | Loss |
POGZ
PSMB4
SELENBP1
|
| esv2758969 | Chr.1:151356318 - 151439159 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| esv3587525 | Chr.1:151360256 - 151412906 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| nsv824575 | Chr.1:151359057 - 151435620 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| nsv4067263 | Chr.1:151359592 - 151435987 on Build GRCh38 | Duplication |
POGZ
PSMB4
SELENBP1
|
| esv34461 | Chr.1:151268066 - 151439159 on Build GRCh38 | Gain |
ZNF687-AS1
RFX5-AS1
POGZ
RFX5
PI4KB
ZNF687
PSMB4
SELENBP1
|
| nsv1161560 | Chr.1:151359541 - 151436260 on Build GRCh38 | Duplication |
POGZ
PSMB4
SELENBP1
|
| dgv76n145 | Chr.1:151358895 - 151432320 on Build GRCh38 | Duplication |
POGZ
PSMB4
SELENBP1
|
| nsv5981509 | Chr.1:151359872 - 151436237 on Build GRCh38 | Duplication |
POGZ
PSMB4
SELENBP1
|
| esv3894200 | Chr.1:151360691 - 151435217 on Build GRCh38 | Gain |
POGZ
PSMB4
SELENBP1
|
| nsv438026 | Chr.1:151346257 - 151372227 on Build GRCh38 | Loss |
RFX5-AS1
RFX5
SELENBP1
|
| nsv4062004 | Chr.1:151356470 - 151369416 on Build GRCh38 | Duplication |
SELENBP1
|
| nsv6138677 | Chr.1:151359589 - 151436025 on Build GRCh38 | Duplication |
POGZ
PSMB4
SELENBP1
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs72710112] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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