BAD BCL2 associated agonist of cell death

Information
Symbol
BAD
Type
protein-coding
Description
BCL2 associated agonist of cell death
Entrez Gene ID
572
Genome
hg19
Position
chr11:64,037,302-64,052,111
Genome
hg38
Position
chr11:64,269,830-64,284,639
MIM
603167 OMIM
HGNC
HGNC:936 HGNC
Ensembl
ENSG00000002330 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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 BBC2
SYNONYM BCL2L8
MIM 603167 OMIM
HGNC HGNC:936 HGNC
Ensembl ENSG00000002330 Ensembl
AllianceGenome HGNC:936
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544785.1 hg38 chr11 64,270,001 64,284,369 14,369
ENST00000309032.8 hg38 chr11 64,269,830 64,284,665 14,836
ENST00000394531.3 hg38 chr11 64,270,256 64,284,653 14,398
ENST00000394532.7 hg38 chr11 64,269,830 64,284,639 14,810
ENST00000394532.7 hg19 chr11 64,037,302 64,052,111 14,810
ENST00000309032.8 hg19 chr11 64,037,302 64,052,137 14,836
ENST00000544785.1 hg19 chr11 64,037,473 64,051,841 14,369
ENST00000394531.3 hg19 chr11 64,037,728 64,052,125 14,398
Genome browser