BHLHE22 basic helix-loop-helix family member e22

Information
Symbol
BHLHE22
Type
protein-coding
Description
basic helix-loop-helix family member e22
Entrez Gene ID
27319
Genome
hg19
Position
chr8:65,492,922-65,496,184
Genome
hg38
Position
chr8:64,580,365-64,583,627
MIM
613483 OMIM
HGNC
HGNC:11963 HGNC
Ensembl
ENSG00000180828 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
66
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
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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 :
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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 :
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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 BHLHB5
SYNONYM Beta3
SYNONYM Beta3a
SYNONYM CAGL85
SYNONYM TNRC20
MIM 613483 OMIM
HGNC HGNC:11963 HGNC
Ensembl ENSG00000180828 Ensembl
AllianceGenome HGNC:11963
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000321870.3 hg38 chr8 64,580,365 64,583,627 3,263
ENST00000321870.3 hg19 chr8 65,492,922 65,496,184 3,263
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