EMX1 empty spiracles homeobox 1

Information
Symbol
EMX1
Type
protein-coding
Description
empty spiracles homeobox 1
Entrez Gene ID
2016
Genome
hg19
Position
chr2:73,144,648-73,162,020
Genome
hg38
Position
chr2:72,917,519-72,934,891
MIM
600034 OMIM
HGNC
HGNC:3340 HGNC
Ensembl
ENSG00000135638 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
32
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
MIM 600034 OMIM
HGNC HGNC:3340 HGNC
Ensembl ENSG00000135638 Ensembl
AllianceGenome HGNC:3340
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000394111.6 hg38 chr2 72,916,260 72,934,328 18,069
ENST00000258106.11 hg38 chr2 72,917,519 72,934,891 17,373
ENST00000394111.6 hg19 chr2 73,143,389 73,161,457 18,069
ENST00000258106.11 hg19 chr2 73,144,648 73,162,020 17,373
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