IFRD2 interferon related developmental regulator 2
Information
- Symbol
- IFRD2
- Type
- protein-coding
- Description
- interferon related developmental regulator 2
- Entrez Gene ID
- 7866
- Genome
- hg19
- Position
- chr3:50,325,174-50,330,349
- Genome
- hg38
- Position
- chr3:50,287,743-50,292,918
- MIM
- 602725 OMIM
- HGNC
- HGNC:5457 HGNC
- Ensembl
- ENSG00000214706 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 82 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
2 |
![]() |
84 |
![]() |
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
[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 | |||||||||||
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 | IFNRP |
| SYNONYM | SKMc15 |
| SYNONYM | SM15 |
| MIM | 602725 OMIM |
| HGNC | HGNC:5457 HGNC |
| Ensembl | ENSG00000214706 Ensembl |
| AllianceGenome | HGNC:5457 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000417626.8 | hg38 | chr3 | 50,287,732 | 50,292,429 | 4,698 |
| ENST00000436390.5 | hg38 | chr3 | 50,287,743 | 50,292,918 | 5,176 |
| ENST00000417626.8 | hg19 | chr3 | 50,325,163 | 50,329,860 | 4,698 |
| ENST00000436390.5 | hg19 | chr3 | 50,325,174 | 50,330,349 | 5,176 |
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