EIF4E2 eukaryotic translation initiation factor 4E family member 2
Information
- Symbol
- EIF4E2
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 4E family member 2
- Entrez Gene ID
- 9470
- Genome
- hg19
- Position
- chr2:233,415,399-233,433,920
- Genome
- hg38
- Position
- chr2:232,550,689-232,569,210
- MIM
- 605895 OMIM
- HGNC
- HGNC:3293 HGNC
- Ensembl
- ENSG00000135930 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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30 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | 4E-LP |
SYNONYM | 4EHP |
SYNONYM | EIF4EL3 |
SYNONYM | IF4e |
SYNONYM | h4EHP |
MIM | 605895 OMIM |
HGNC | HGNC:3293 HGNC |
Ensembl | ENSG00000135930 Ensembl |
AllianceGenome | HGNC:3293 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409098.5 | hg38 | chr2 | 232,550,683 | 232,583,644 | 32,962 |
ENST00000687222.1 | hg38 | chr2 | 232,550,659 | 232,583,616 | 32,958 |
ENST00000409495.6 | hg38 | chr2 | 232,550,689 | 232,569,206 | 18,518 |
ENST00000258416.8 | hg38 | chr2 | 232,550,689 | 232,569,210 | 18,522 |
ENST00000409167.8 | hg38 | chr2 | 232,550,689 | 232,569,198 | 18,510 |
ENST00000690794.1 | hg38 | chr2 | 232,550,677 | 232,583,584 | 32,908 |
ENST00000409394.5 | hg38 | chr2 | 232,550,704 | 232,580,956 | 30,253 |
ENST00000409514.5 | hg38 | chr2 | 232,550,683 | 232,583,642 | 32,960 |
ENST00000409322.5 | hg38 | chr2 | 232,550,692 | 232,569,178 | 18,487 |
ENST00000409514.5 | hg19 | chr2 | 233,415,393 | 233,448,352 | 32,960 |
ENST00000687222.1 | hg19 | chr2 | 233,415,369 | 233,448,326 | 32,958 |
ENST00000409098.5 | hg19 | chr2 | 233,415,393 | 233,448,354 | 32,962 |
ENST00000409167.8 | hg19 | chr2 | 233,415,399 | 233,433,908 | 18,510 |
ENST00000409495.6 | hg19 | chr2 | 233,415,399 | 233,433,916 | 18,518 |
ENST00000258416.8 | hg19 | chr2 | 233,415,399 | 233,433,920 | 18,522 |
ENST00000409322.5 | hg19 | chr2 | 233,415,402 | 233,433,888 | 18,487 |
ENST00000409394.5 | hg19 | chr2 | 233,415,414 | 233,445,666 | 30,253 |
ENST00000690794.1 | hg19 | chr2 | 233,415,387 | 233,448,294 | 32,908 |
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