BIN2 bridging integrator 2

Information
Symbol
BIN2
Type
protein-coding
Description
bridging integrator 2
Entrez Gene ID
51411
Genome
hg19
Position
chr12:51,674,822-51,717,958
Genome
hg38
Position
chr12:51,281,038-51,324,174
MIM
605936 OMIM
HGNC
HGNC:1053 HGNC
Ensembl
ENSG00000110934 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
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
[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 BRAP-1
MIM 605936 OMIM
HGNC HGNC:1053 HGNC
Ensembl ENSG00000110934 Ensembl
AllianceGenome HGNC:1053
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000452142.7 hg38 chr12 51,281,038 51,324,154 43,117
ENST00000544402.5 hg38 chr12 51,281,282 51,324,668 43,387
ENST00000615107.6 hg38 chr12 51,281,038 51,324,174 43,137
ENST00000604560.6 hg38 chr12 51,281,038 51,324,115 43,078
ENST00000604560.6 hg19 chr12 51,674,822 51,717,899 43,078
ENST00000452142.7 hg19 chr12 51,674,822 51,717,938 43,117
ENST00000615107.6 hg19 chr12 51,674,822 51,717,958 43,137
ENST00000544402.5 hg19 chr12 51,675,066 51,718,452 43,387
Genome browser