IL1RL2 interleukin 1 receptor like 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 10 |
association | 0 | 4 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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78 |
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4 |
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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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 | |||||
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | IL-1Rrp2 |
SYNONYM | IL-36R |
SYNONYM | IL1R-rp2 |
SYNONYM | IL1RRP2 |
MIM | 604512 OMIM |
HGNC | HGNC:5999 HGNC |
Ensembl | ENSG00000115598 Ensembl |
AllianceGenome | HGNC:5999 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000264257.7 | hg38 | chr2 | 102,187,023 | 102,240,002 | 52,980 |
ENST00000441515.3 | hg38 | chr2 | 102,187,015 | 102,239,351 | 52,337 |
ENST00000441515.3 | hg19 | chr2 | 102,803,475 | 102,855,811 | 52,337 |
ENST00000264257.7 | hg19 | chr2 | 102,803,483 | 102,856,462 | 52,980 |
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