EVX2 even-skipped homeobox 2

Information
Symbol
EVX2
Type
protein-coding
Description
even-skipped homeobox 2
Entrez Gene ID
344191
Genome
hg19
Position
chr2:176,942,200-176,948,690
Genome
hg38
Position
chr2:176,077,472-176,083,962
MIM
142991 OMIM
HGNC
HGNC:3507 HGNC
Ensembl
ENSG00000174279 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
not provided 1 0
Uncertain significance 0 68
Ranking
ClinVar
0
0
2
78
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 :
Filtering :
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 EVX-2
MIM 142991 OMIM
HGNC HGNC:3507 HGNC
Ensembl ENSG00000174279 Ensembl
AllianceGenome HGNC:3507
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308618.5 hg38 chr2 176,077,472 176,083,962 6,491
ENST00000308618.5 hg19 chr2 176,942,200 176,948,690 6,491
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