HHEX hematopoietically expressed homeobox

Information
Symbol
HHEX
Type
protein-coding
Description
hematopoietically expressed homeobox
Entrez Gene ID
3087
Genome
hg19
Position
chr10:94,449,712-94,455,404
Genome
hg38
Position
chr10:92,689,955-92,695,647
MIM
604420 OMIM
HGNC
HGNC:4901 HGNC
Ensembl
ENSG00000152804 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
30
2
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 HEX
SYNONYM HMPH
SYNONYM HOX11L-PEN
SYNONYM PRH
SYNONYM PRHX
MIM 604420 OMIM
HGNC HGNC:4901 HGNC
Ensembl ENSG00000152804 Ensembl
AllianceGenome HGNC:4901
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000472590.6 hg38 chr10 92,691,820 92,695,641 3,822
ENST00000492654.3 hg38 chr10 92,692,032 92,694,788 2,757
ENST00000282728.10 hg38 chr10 92,689,955 92,695,647 5,693
ENST00000282728.10 hg19 chr10 94,449,712 94,455,404 5,693
ENST00000472590.6 hg19 chr10 94,451,577 94,455,398 3,822
ENST00000492654.3 hg19 chr10 94,451,789 94,454,545 2,757
Genome browser