EFNB2 ephrin B2

Information
Symbol
EFNB2
Type
protein-coding
Description
ephrin B2
Entrez Gene ID
1948
Genome
hg19
Position
chr13:107,142,093-107,188,010
Genome
hg38
Position
chr13:106,489,745-106,535,662
MIM
600527 OMIM
HGNC
HGNC:3227 HGNC
Ensembl
ENSG00000125266 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Likely benign 0 12
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
34
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 :
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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 EPLG5
SYNONYM HTKL
SYNONYM Htk-L
SYNONYM LERK5
SYNONYM ephrin-B2
MIM 600527 OMIM
HGNC HGNC:3227 HGNC
Ensembl ENSG00000125266 Ensembl
AllianceGenome HGNC:3227
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000646441.1 hg38 chr13 106,489,745 106,535,662 45,918
ENST00000646441.1 hg19 chr13 107,142,093 107,188,010 45,918
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