IL18RAP interleukin 18 receptor accessory protein
Information
- Symbol
- IL18RAP
- Type
- protein-coding
- Description
- interleukin 18 receptor accessory protein
- Entrez Gene ID
- 8807
- Genome
- hg19
- Position
- chr2:103,035,149-103,069,025
- Genome
- hg38
- Position
- chr2:102,418,689-102,452,565
- MIM
- 604509 OMIM
- HGNC
- HGNC:5989 HGNC
- Ensembl
- ENSG00000115607 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 14 |
association | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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54 |
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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
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 | |||||
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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 |
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 | ACPL |
SYNONYM | CD218b |
SYNONYM | CDw218b |
SYNONYM | IL-18R-beta |
SYNONYM | IL-18RAcP |
SYNONYM | IL-18Rbeta |
SYNONYM | IL-1R-7 |
SYNONYM | IL-1R7 |
SYNONYM | IL-1RAcPL |
SYNONYM | IL18RB |
MIM | 604509 OMIM |
HGNC | HGNC:5989 HGNC |
Ensembl | ENSG00000115607 Ensembl |
AllianceGenome | HGNC:5989 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409369.1 | hg38 | chr2 | 102,419,686 | 102,452,384 | 32,699 |
ENST00000264260.6 | hg38 | chr2 | 102,418,689 | 102,452,565 | 33,877 |
ENST00000687160.1 | hg38 | chr2 | 102,423,160 | 102,452,565 | 29,406 |
ENST00000264260.6 | hg19 | chr2 | 103,035,149 | 103,069,025 | 33,877 |
ENST00000409369.1 | hg19 | chr2 | 103,036,146 | 103,068,844 | 32,699 |
ENST00000687160.1 | hg19 | chr2 | 103,039,620 | 103,069,025 | 29,406 |
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