EIF4ENIF1 eukaryotic translation initiation factor 4E nuclear import factor 1

Information
Symbol
EIF4ENIF1
Type
protein-coding
Description
eukaryotic translation initiation factor 4E nuclear import factor 1
Entrez Gene ID
56478
Genome
hg19
Position
chr22:31,835,353-31,885,573
Genome
hg38
Position
chr22:31,439,367-31,489,587
MIM
607445 OMIM
HGNC
HGNC:16687 HGNC
Ensembl
ENSG00000184708 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
118
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
Category :
Search word :
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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
Category :
Search word :
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
Category :
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
TypeID
SYNONYM 4E-T
SYNONYM Clast4
MIM 607445 OMIM
HGNC HGNC:16687 HGNC
Ensembl ENSG00000184708 Ensembl
AllianceGenome HGNC:16687
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397525.5 hg38 chr22 31,439,367 31,489,587 50,221
ENST00000397523.5 hg38 chr22 31,439,373 31,488,745 49,373
ENST00000330125.10 hg38 chr22 31,439,367 31,489,842 50,476
ENST00000344710.9 hg38 chr22 31,439,359 31,489,824 50,466
ENST00000344710.9 hg19 chr22 31,835,345 31,885,810 50,466
ENST00000397525.5 hg19 chr22 31,835,353 31,885,573 50,221
ENST00000330125.10 hg19 chr22 31,835,353 31,885,828 50,476
ENST00000397523.5 hg19 chr22 31,835,359 31,884,731 49,373
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