IL13RA1 interleukin 13 receptor subunit alpha 1
Information
- Symbol
- IL13RA1
- Type
- protein-coding
- Description
- interleukin 13 receptor subunit alpha 1
- Entrez Gene ID
- 3597
- Genome
- hg19
- Position
- chrX:117,861,569-117,928,496
- Genome
- hg38
- Position
- chrX:118,727,606-118,794,533
- MIM
- 300119 OMIM
- HGNC
- HGNC:5974 HGNC
- Ensembl
- ENSG00000131724 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 10 |
not provided | 6 | 0 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
40 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | CD213A1 |
SYNONYM | CT19 |
SYNONYM | IL-13Ra |
SYNONYM | NR4 |
MIM | 300119 OMIM |
HGNC | HGNC:5974 HGNC |
Ensembl | ENSG00000131724 Ensembl |
AllianceGenome | HGNC:5974 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000652600.1 | hg38 | chrX | 118,727,133 | 118,794,535 | 67,403 |
ENST00000371642.1 | hg38 | chrX | 118,727,602 | 118,761,520 | 33,919 |
ENST00000371666.8 | hg38 | chrX | 118,727,606 | 118,794,533 | 66,928 |
ENST00000652600.1 | hg19 | chrX | 117,861,096 | 117,928,498 | 67,403 |
ENST00000371642.1 | hg19 | chrX | 117,861,565 | 117,895,483 | 33,919 |
ENST00000371666.8 | hg19 | chrX | 117,861,569 | 117,928,496 | 66,928 |
Genome browser