IRGQ immunity related GTPase Q
Information
- Symbol
- IRGQ
- Type
- protein-coding
- Description
- immunity related GTPase Q
- Entrez Gene ID
- 126298
- Genome
- hg19
- Position
- chr19:44,088,519-44,100,286
- Genome
- hg38
- Position
- chr19:43,584,367-43,596,134
- HGNC
- HGNC:24868 HGNC
- Ensembl
- ENSG00000167378 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
| Uncertain significance | 0 | 52 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
50 |
 |
2 |
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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| 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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| 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 | FKSG27 |
| SYNONYM | IRGQ1 |
| HGNC | HGNC:24868 HGNC |
| Ensembl | ENSG00000167378 Ensembl |
| AllianceGenome | HGNC:24868 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000602269.2 | hg38 | chr19 | 43,585,936 | 43,595,524 | 9,589 |
| ENST00000422989.6 | hg38 | chr19 | 43,584,367 | 43,596,134 | 11,768 |
| ENST00000422989.6 | hg19 | chr19 | 44,088,519 | 44,100,286 | 11,768 |
| ENST00000602269.2 | hg19 | chr19 | 44,090,088 | 44,099,676 | 9,589 |
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