HLX H2.0 like homeobox

Information
Symbol
HLX
Type
protein-coding
Description
H2.0 like homeobox
Entrez Gene ID
3142
Genome
hg19
Position
chr1:221,052,785-221,058,401
Genome
hg38
Position
chr1:220,879,443-220,885,059
MIM
142995 OMIM
HGNC
HGNC:4978 HGNC
Ensembl
ENSG00000136630 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
not provided 1 0
Uncertain significance 0 44
Ranking
ClinVar
0
0
2
50
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 HB24
SYNONYM HLX1
MIM 142995 OMIM
HGNC HGNC:4978 HGNC
Ensembl ENSG00000136630 Ensembl
AllianceGenome HGNC:4978
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000366903.8 hg38 chr1 220,879,443 220,885,059 5,617
ENST00000366903.8 hg19 chr1 221,052,785 221,058,401 5,617
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