IFI27L2 interferon alpha inducible protein 27 like 2
Information
- Symbol
- IFI27L2
- Type
- protein-coding
- Description
- interferon alpha inducible protein 27 like 2
- Entrez Gene ID
- 83982
- Genome
- hg19
- Position
- chr14:94,594,118-94,595,941
- Genome
- hg38
- Position
- chr14:94,127,781-94,129,604
- MIM
- 611319 OMIM
- HGNC
- HGNC:19753 HGNC
- Ensembl
- ENSG00000119632 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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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| 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 | FAM14A |
| SYNONYM | ISG12B |
| SYNONYM | TLH29 |
| MIM | 611319 OMIM |
| HGNC | HGNC:19753 HGNC |
| Ensembl | ENSG00000119632 Ensembl |
| AllianceGenome | HGNC:19753 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000238609.4 | hg38 | chr14 | 94,127,781 | 94,129,604 | 1,824 |
| ENST00000556727.1 | hg38 | chr14 | 94,127,789 | 94,130,253 | 2,465 |
| ENST00000238609.4 | hg19 | chr14 | 94,594,118 | 94,595,941 | 1,824 |
| ENST00000556727.1 | hg19 | chr14 | 94,594,126 | 94,596,590 | 2,465 |
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