HDX highly divergent homeobox

Information
Symbol
HDX
Type
protein-coding
Description
highly divergent homeobox
Entrez Gene ID
139324
Genome
hg19
Position
chrX:83,572,886-83,757,461
Genome
hg38
Position
chrX:84,317,878-84,502,453
MIM
300994 OMIM
HGNC
HGNC:26411 HGNC
Ensembl
ENSG00000165259 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 2
not provided 6 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
54
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 CXorf43
SYNONYM D030011N01Rik
MIM 300994 OMIM
HGNC HGNC:26411 HGNC
Ensembl ENSG00000165259 Ensembl
AllianceGenome HGNC:26411
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000506585.6 hg38 chrX 84,317,878 84,502,453 184,576
ENST00000297977.9 hg38 chrX 84,317,874 84,502,453 184,580
ENST00000373177.3 hg38 chrX 84,317,878 84,502,453 184,576
ENST00000297977.9 hg19 chrX 83,572,882 83,757,461 184,580
ENST00000506585.6 hg19 chrX 83,572,886 83,757,461 184,576
ENST00000373177.3 hg19 chrX 83,572,886 83,757,461 184,576
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