EIF4G2 eukaryotic translation initiation factor 4 gamma 2
Information
- Symbol
- EIF4G2
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 4 gamma 2
- Entrez Gene ID
- 1982
- Genome
- hg19
- Position
- chr11:10,818,597-10,829,520
- Genome
- hg38
- Position
- chr11:10,797,050-10,807,973
- MIM
- 602325 OMIM
- HGNC
- HGNC:3297 HGNC
- Ensembl
- ENSG00000110321 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
44 |
 |
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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| 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 | AAG1 |
| SYNONYM | DAP5 |
| SYNONYM | NAT1 |
| SYNONYM | P97 |
| MIM | 602325 OMIM |
| HGNC | HGNC:3297 HGNC |
| Ensembl | ENSG00000110321 Ensembl |
| AllianceGenome | HGNC:3297 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396525.7 | hg38 | chr11 | 10,797,170 | 10,808,708 | 11,539 |
| ENST00000339995.11 | hg38 | chr11 | 10,797,054 | 10,808,926 | 11,873 |
| ENST00000525681.6 | hg38 | chr11 | 10,797,053 | 10,807,462 | 10,410 |
| ENST00000526148.6 | hg38 | chr11 | 10,797,050 | 10,807,973 | 10,924 |
| ENST00000525681.6 | hg19 | chr11 | 10,818,600 | 10,829,009 | 10,410 |
| ENST00000339995.11 | hg19 | chr11 | 10,818,601 | 10,830,473 | 11,873 |
| ENST00000396525.7 | hg19 | chr11 | 10,818,717 | 10,830,255 | 11,539 |
| ENST00000526148.6 | hg19 | chr11 | 10,818,597 | 10,829,520 | 10,924 |
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