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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 |
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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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