IL1RL1 interleukin 1 receptor like 1
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 18 |
| Likely benign | 0 | 20 |
| association | 0 | 10 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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6 |
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86 |
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10 |
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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| Target data | : |
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 | DER4 |
| SYNONYM | FIT-1 |
| SYNONYM | IL33R |
| SYNONYM | ST2 |
| SYNONYM | ST2L |
| SYNONYM | ST2V |
| SYNONYM | T1 |
| MIM | 601203 OMIM |
| HGNC | HGNC:5998 HGNC |
| Ensembl | ENSG00000115602 Ensembl |
| AllianceGenome | HGNC:5998 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000233954.6 | hg38 | chr2 | 102,311,563 | 102,352,037 | 40,475 |
| ENST00000409584.5 | hg38 | chr2 | 102,337,258 | 102,344,951 | 7,694 |
| ENST00000311734.6 | hg38 | chr2 | 102,337,148 | 102,346,100 | 8,953 |
| ENST00000404917.6 | hg38 | chr2 | 102,311,502 | 102,346,099 | 34,598 |
| ENST00000404917.6 | hg19 | chr2 | 102,927,962 | 102,962,559 | 34,598 |
| ENST00000233954.6 | hg19 | chr2 | 102,928,023 | 102,968,497 | 40,475 |
| ENST00000311734.6 | hg19 | chr2 | 102,953,608 | 102,962,560 | 8,953 |
| ENST00000409584.5 | hg19 | chr2 | 102,953,718 | 102,961,411 | 7,694 |
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