IL1RN interleukin 1 receptor antagonist
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 14 |
| Likely pathogenic | 0 | 8 |
| Benign | 0 | 88 |
| Likely benign | 0 | 122 |
| Conflicting classifications of pathogenicity | 0 | 26 |
| Uncertain significance | 0 | 174 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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70 |
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326 |
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2 |
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
Search Word
| Target data | : |
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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MGeND data only
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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 | ||||||||||||||
Search Word
| Target data | : |
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 | CRMO2 |
| SYNONYM | DIRA |
| SYNONYM | ICIL-1RA |
| SYNONYM | IL-1RN |
| SYNONYM | IL-1ra |
| SYNONYM | IL-1ra3 |
| SYNONYM | IL1F3 |
| SYNONYM | IL1RA |
| SYNONYM | IRAP |
| SYNONYM | MVCD4 |
| MIM | 147679 OMIM |
| HGNC | HGNC:6000 HGNC |
| Ensembl | ENSG00000136689 Ensembl |
| AllianceGenome | HGNC:6000 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000409930.4 | hg38 | chr2 | 113,127,598 | 113,134,014 | 6,417 |
| ENST00000696879.1 | hg38 | chr2 | 113,127,483 | 113,133,536 | 6,054 |
| ENST00000354115.6 | hg38 | chr2 | 113,117,897 | 113,134,016 | 16,120 |
| ENST00000696881.1 | hg38 | chr2 | 113,117,941 | 113,133,001 | 15,061 |
| ENST00000259206.9 | hg38 | chr2 | 113,117,897 | 113,134,016 | 16,120 |
| ENST00000361779.7 | hg38 | chr2 | 113,117,893 | 113,134,016 | 16,124 |
| ENST00000361779.7 | hg19 | chr2 | 113,875,470 | 113,891,593 | 16,124 |
| ENST00000259206.9 | hg19 | chr2 | 113,875,474 | 113,891,593 | 16,120 |
| ENST00000354115.6 | hg19 | chr2 | 113,875,474 | 113,891,593 | 16,120 |
| ENST00000696881.1 | hg19 | chr2 | 113,875,518 | 113,890,578 | 15,061 |
| ENST00000696879.1 | hg19 | chr2 | 113,885,060 | 113,891,113 | 6,054 |
| ENST00000409930.4 | hg19 | chr2 | 113,885,175 | 113,891,591 | 6,417 |
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