IL23R interleukin 23 receptor
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 48 |
| Likely benign | 0 | 236 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 314 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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40 |
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544 |
![]() |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | PSORS7 |
| MIM | 607562 OMIM |
| HGNC | HGNC:19100 HGNC |
| Ensembl | ENSG00000162594 Ensembl |
| AllianceGenome | HGNC:19100 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000347310.10 | hg38 | chr1 | 67,166,454 | 67,259,979 | 93,526 |
| ENST00000697154.1 | hg38 | chr1 | 67,168,121 | 67,258,577 | 90,457 |
| ENST00000697164.1 | hg38 | chr1 | 67,168,121 | 67,259,128 | 91,008 |
| ENST00000697163.1 | hg38 | chr1 | 67,168,121 | 67,258,577 | 90,457 |
| ENST00000697165.1 | hg38 | chr1 | 67,168,121 | 67,259,128 | 91,008 |
| ENST00000697222.1 | hg38 | chr1 | 67,138,987 | 67,170,708 | 31,722 |
| ENST00000425614.3 | hg38 | chr1 | 67,207,616 | 67,259,248 | 51,633 |
| ENST00000697230.1 | hg38 | chr1 | 67,168,121 | 67,258,577 | 90,457 |
| ENST00000347310.10 | hg19 | chr1 | 67,632,137 | 67,725,662 | 93,526 |
| ENST00000697154.1 | hg19 | chr1 | 67,633,804 | 67,724,260 | 90,457 |
| ENST00000697163.1 | hg19 | chr1 | 67,633,804 | 67,724,260 | 90,457 |
| ENST00000425614.3 | hg19 | chr1 | 67,673,299 | 67,724,931 | 51,633 |
| ENST00000697230.1 | hg19 | chr1 | 67,633,804 | 67,724,260 | 90,457 |
| ENST00000697164.1 | hg19 | chr1 | 67,633,804 | 67,724,811 | 91,008 |
| ENST00000697165.1 | hg19 | chr1 | 67,633,804 | 67,724,811 | 91,008 |
| ENST00000697222.1 | hg19 | chr1 | 67,604,670 | 67,636,391 | 31,722 |
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