EIF3L eukaryotic translation initiation factor 3 subunit L
Information
- Symbol
- EIF3L
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 3 subunit L
- Entrez Gene ID
- 51386
- Genome
- hg19
- Position
- chr22:38,245,426-38,285,414
- Genome
- hg38
- Position
- chr22:37,849,419-37,889,407
- MIM
- 619197 OMIM
- HGNC
- HGNC:18138 HGNC
- Ensembl
- ENSG00000100129 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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 |
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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 | |||
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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 | EIF3EIP |
SYNONYM | EIF3S11 |
SYNONYM | EIF3S6IP |
SYNONYM | HSPC021 |
SYNONYM | HSPC025 |
SYNONYM | MSTP005 |
MIM | 619197 OMIM |
HGNC | HGNC:18138 HGNC |
Ensembl | ENSG00000100129 Ensembl |
AllianceGenome | HGNC:18138 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000624234.3 | hg38 | chr22 | 37,849,372 | 37,888,782 | 39,411 |
ENST00000412331.6 | hg38 | chr22 | 37,848,868 | 37,889,407 | 40,540 |
ENST00000652021.1 | hg38 | chr22 | 37,849,419 | 37,889,407 | 39,989 |
ENST00000406934.5 | hg38 | chr22 | 37,849,481 | 37,888,630 | 39,150 |
ENST00000381683.10 | hg38 | chr22 | 37,849,417 | 37,888,479 | 39,063 |
ENST00000412331.6 | hg19 | chr22 | 38,244,875 | 38,285,414 | 40,540 |
ENST00000624234.3 | hg19 | chr22 | 38,245,379 | 38,284,789 | 39,411 |
ENST00000381683.10 | hg19 | chr22 | 38,245,424 | 38,284,486 | 39,063 |
ENST00000652021.1 | hg19 | chr22 | 38,245,426 | 38,285,414 | 39,989 |
ENST00000406934.5 | hg19 | chr22 | 38,245,488 | 38,284,637 | 39,150 |
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