IL18 interleukin 18
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 4 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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10 |
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6 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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MGeND data only
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
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MGeND data only
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| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | IGIF |
| SYNONYM | IL-18 |
| SYNONYM | IL-1g |
| SYNONYM | IL1F4 |
| MIM | 600953 OMIM |
| HGNC | HGNC:5986 HGNC |
| Ensembl | ENSG00000150782 Ensembl |
| AllianceGenome | HGNC:5986 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000524595.5 | hg38 | chr11 | 112,143,253 | 112,164,074 | 20,822 |
| ENST00000280357.12 | hg38 | chr11 | 112,143,260 | 112,164,094 | 20,835 |
| ENST00000528832.1 | hg38 | chr11 | 112,143,596 | 112,164,089 | 20,494 |
| ENST00000524595.5 | hg19 | chr11 | 112,013,976 | 112,034,797 | 20,822 |
| ENST00000280357.12 | hg19 | chr11 | 112,013,983 | 112,034,817 | 20,835 |
| ENST00000528832.1 | hg19 | chr11 | 112,014,319 | 112,034,812 | 20,494 |
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