IL13RA2 interleukin 13 receptor subunit alpha 2
Information
- Symbol
- IL13RA2
- Type
- protein-coding
- Description
- interleukin 13 receptor subunit alpha 2
- Entrez Gene ID
- 3598
- Genome
- hg19
- Position
- chrX:114,238,538-114,253,536
- Genome
- hg38
- Position
- chrX:115,003,975-115,018,973
- MIM
- 300130 OMIM
- HGNC
- HGNC:5975 HGNC
- Ensembl
- ENSG00000123496 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 7 | 0 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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14 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | |||||||||||
Search Word
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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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| Category | : |
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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 | CD213A2 |
| SYNONYM | CT19 |
| SYNONYM | IL-13R |
| SYNONYM | IL13BP |
| MIM | 300130 OMIM |
| HGNC | HGNC:5975 HGNC |
| Ensembl | ENSG00000123496 Ensembl |
| AllianceGenome | HGNC:5975 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000371936.5 | hg38 | chrX | 115,003,975 | 115,018,973 | 14,999 |
| ENST00000243213.2 | hg38 | chrX | 115,003,982 | 115,017,616 | 13,635 |
| ENST00000371936.5 | hg19 | chrX | 114,238,538 | 114,253,536 | 14,999 |
| ENST00000243213.2 | hg19 | chrX | 114,238,545 | 114,252,179 | 13,635 |
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