HEXIM2 HEXIM P-TEFb complex subunit 2

Information
Symbol
HEXIM2
Type
protein-coding
Description
HEXIM P-TEFb complex subunit 2
Entrez Gene ID
124790
Genome
hg19
Position
chr17:43,238,067-43,247,407
Genome
hg38
Position
chr17:45,160,700-45,170,040
MIM
615695 OMIM
HGNC
HGNC:28591 HGNC
Ensembl
ENSG00000168517 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
SYNONYM L3
MIM 615695 OMIM
HGNC HGNC:28591 HGNC
Ensembl ENSG00000168517 Ensembl
AllianceGenome HGNC:28591
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000592695.1 hg38 chr17 45,161,917 45,170,035 8,119
ENST00000591576.5 hg38 chr17 45,161,895 45,170,035 8,141
ENST00000307275.7 hg38 chr17 45,160,700 45,170,040 9,341
ENST00000589230.6 hg38 chr17 45,161,875 45,170,035 8,161
ENST00000307275.7 hg19 chr17 43,238,067 43,247,407 9,341
ENST00000589230.6 hg19 chr17 43,239,242 43,247,402 8,161
ENST00000591576.5 hg19 chr17 43,239,262 43,247,402 8,141
ENST00000592695.1 hg19 chr17 43,239,284 43,247,402 8,119
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