ELF5 E74 like ETS transcription factor 5

Information
Symbol
ELF5
Type
protein-coding
Description
E74 like ETS transcription factor 5
Entrez Gene ID
2001
Genome
hg19
Position
chr11:34,500,343-34,533,346
Genome
hg38
Position
chr11:34,478,796-34,511,799
MIM
605169 OMIM
HGNC
HGNC:3320 HGNC
Ensembl
ENSG00000135374 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
36
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
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 ESE2
MIM 605169 OMIM
HGNC HGNC:3320 HGNC
Ensembl ENSG00000135374 Ensembl
AllianceGenome HGNC:3320
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000257832.7 hg38 chr11 34,478,791 34,513,794 35,004
ENST00000429939.6 hg38 chr11 34,480,197 34,513,805 33,609
ENST00000620316.4 hg38 chr11 34,478,795 34,511,799 33,005
ENST00000312319.6 hg38 chr11 34,478,796 34,511,799 33,004
ENST00000673820.1 hg38 chr11 34,480,111 34,525,193 45,083
ENST00000532417.1 hg38 chr11 34,491,597 34,513,765 22,169
ENST00000257832.7 hg19 chr11 34,500,338 34,535,341 35,004
ENST00000620316.4 hg19 chr11 34,500,342 34,533,346 33,005
ENST00000312319.6 hg19 chr11 34,500,343 34,533,346 33,004
ENST00000673820.1 hg19 chr11 34,501,658 34,546,740 45,083
ENST00000429939.6 hg19 chr11 34,501,744 34,535,352 33,609
ENST00000532417.1 hg19 chr11 34,513,144 34,535,312 22,169
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