MEOX1 mesenchyme homeobox 1

Information
Symbol
MEOX1
Type
protein-coding
Description
mesenchyme homeobox 1
Entrez Gene ID
4222
Genome
hg19
Position
chr17:41,717,757-41,739,290
Genome
hg38
Position
chr17:43,640,389-43,661,922
MIM
600147 OMIM
HGNC
HGNC:7013 HGNC
Ensembl
ENSG00000005102 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 2
Benign 0 22
Likely benign 0 64
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 96
Ranking
ClinVar
0
0
22
162
4
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 KFS2
SYNONYM MOX1
MIM 600147 OMIM
HGNC HGNC:7013 HGNC
Ensembl ENSG00000005102 Ensembl
AllianceGenome HGNC:7013
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393661.2 hg38 chr17 43,641,380 43,661,922 20,543
ENST00000318579.9 hg38 chr17 43,640,389 43,661,922 21,534
ENST00000549132.2 hg38 chr17 43,641,379 43,661,563 20,185
ENST00000318579.9 hg19 chr17 41,717,757 41,739,290 21,534
ENST00000549132.2 hg19 chr17 41,718,747 41,738,931 20,185
ENST00000393661.2 hg19 chr17 41,718,748 41,739,290 20,543
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