EVX1 even-skipped homeobox 1

Information
Symbol
EVX1
Type
protein-coding
Description
even-skipped homeobox 1
Entrez Gene ID
2128
Genome
hg19
Position
chr7:27,282,421-27,287,449
Genome
hg38
Position
chr7:27,242,802-27,247,830
MIM
142996 OMIM
HGNC
HGNC:3506 HGNC
Ensembl
ENSG00000106038 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
64
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 :
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-1
MIM 142996 OMIM
HGNC HGNC:3506 HGNC
Ensembl ENSG00000106038 Ensembl
AllianceGenome HGNC:3506
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000496902.7 hg38 chr7 27,242,802 27,247,830 5,029
ENST00000222761.7 hg38 chr7 27,242,700 27,246,425 3,726
ENST00000222761.7 hg19 chr7 27,282,319 27,286,044 3,726
ENST00000496902.7 hg19 chr7 27,282,421 27,287,449 5,029
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