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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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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 |
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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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