Genomic Map
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Target Gene Details
Entrez Gene ID: | 10068 |
Gene Name: | interleukin 18 binding protein |
Gene Aliases: |
IL18BPa |
Location: |
Chr.11:71997944-72002919 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| IL18BP | NM_001039659.1 | 7 | 911 | NP_001034748.1 |
| NM_001039660.1 | 6 | 799 | NP_001034749.1 | |
| NM_001145055.1 | 3 | 419 | NP_001138527.1 | |
| NM_001145057.1 | 6 | 737 | NP_001138529.1 | |
| NM_005699.3 | 4 | 1786 | NP_005690.2 | |
| NM_173042.2 | 5 | 1555 | NP_766630.2 | |
| NM_173044.2 | 6 | 671 | NP_766632.2 | |
| XM_017017059.1 | 6 | 1501 | XP_016872548.1 | |
| XM_017017060.1 | 6 | 1468 | XP_016872549.1 | |
| XM_017017061.1 | 7 | 1364 | XP_016872550.1 | |
| XM_017017062.1 | 7 | 1237 | XP_016872551.1 | |
| XM_017017063.1 | 7 | 1813 | XP_016872552.1 | |
| AB019504.1 | BAA76374.1 | |||
| AF110799.1 | 5 | 692 | AAD17190.1 | |
| AF110800.1 | 3 | 420 | AAD17191.1 | |
| AF110801.1 | 4 | 1786 | AAD17192.1 | |
| AF122906.1 | 6 | 711 | AAD41051.1 | |
| AF215907.2 | 6 | 660 | AAF31697.1 | |
| AK098255.1 | 5 | 2649 | ||
| BC044215.1 | 7 | 893 | AAH44215.1 | |
| BX357194.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428262 | Chr.11:71652593 - 72093009 on Build GRCh38 | Gain+Loss |
 LOC100128494
LOC100129216
NUMA1
MIR3165
ZNF705E
FAM86C1
LOC100133315
IL18BP
RNF121
ALG1L9P
DEFB108B
LRTOMT
|
| nsv951037 | Chr.11:72000055 - 72016354 on Build GRCh38 | Deletion |
LOC100128494
NUMA1
IL18BP
|
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Additional Information:
For this assay, SNP(s) [rs115537466,rs142074822] 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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