IL9R interleukin 9 receptor
Information
- Symbol
- IL9R
- Type
- protein-coding
- Description
- interleukin 9 receptor
- Entrez Gene ID
- 3581
- Genome
- hg19
- Position
- chrX:155,227,361-155,240,482
- Genome
- hg19
- Position
- chrY:59,330,367-59,343,488
- Genome
- hg38
- Position
- chrY:57,184,216-57,197,337
- Genome
- hg38
- Position
- chrX:155,997,696-156,010,817
- MIM
- 300007 OMIM
- HGNC
- HGNC:6030 HGNC
- Ensembl
- ENSG00000124334 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 16 |
| not provided | 1 | 0 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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16 |
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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
| Target data | : |
MGeND data only
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| 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
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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 | CD129 |
| SYNONYM | IL-9R |
| MIM | 300007 OMIM |
| HGNC | HGNC:6030 HGNC |
| Ensembl | ENSG00000124334 Ensembl |
| Ensembl | ENSG00000292373 Ensembl |
| AllianceGenome | HGNC:6030 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000369423.7 | hg38 | chrX | 155,997,706 | 156,010,817 | 13,112 |
| ENST00000711287.1 | hg38 | chrY | 57,184,226 | 57,197,337 | 13,112 |
| ENST00000711286.1 | hg38 | chrY | 57,184,216 | 57,197,337 | 13,122 |
| ENST00000244174.11 | hg38 | chrX | 155,997,696 | 156,010,817 | 13,122 |
| ENST00000244174.11 | hg19 | chrX | 155,227,361 | 155,240,482 | 13,122 |
| ENST00000369423.7 | hg19 | chrX | 155,227,371 | 155,240,482 | 13,112 |
| ENST00000711286.1 | hg19 | chrY | 59,330,367 | 59,343,488 | 13,122 |
| ENST00000711287.1 | hg19 | chrY | 59,330,377 | 59,343,488 | 13,112 |
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