INO80B INO80 complex subunit B

Information
Symbol
INO80B
Type
protein-coding
Description
INO80 complex subunit B
Entrez Gene ID
83444
Genome
hg19
Position
chr2:74,682,214-74,685,071
Genome
hg38
Position
chr2:74,455,087-74,457,944
MIM
616456 OMIM
HGNC
HGNC:13324 HGNC
Ensembl
ENSG00000115274 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
46
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 :
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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 :
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 HMGA1L4
SYNONYM HMGIYL4
SYNONYM IES2
SYNONYM PAP-1BP
SYNONYM PAPA-1
SYNONYM PAPA1
SYNONYM ZNHIT4
SYNONYM hIes2
MIM 616456 OMIM
HGNC HGNC:13324 HGNC
Ensembl ENSG00000115274 Ensembl
AllianceGenome HGNC:13324
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409917.5 hg38 chr2 74,455,102 74,457,662 2,561
ENST00000233331.12 hg38 chr2 74,455,087 74,457,944 2,858
ENST00000233331.12 hg19 chr2 74,682,214 74,685,071 2,858
ENST00000409917.5 hg19 chr2 74,682,229 74,684,789 2,561
KeyValue
strand+
start74,682,149
Gene SymbolINO80B
Entrez GeneId83,444
Chr Band2p13.1
end74,685,086
chrchr2
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