Gene: BAD (BCL2-associated agonist of cell death)  Homo sapiens

Symbol: BAD
Name: BCL2-associated agonist of cell death
Description: The protein encoded by this gene is a member of the BCL-2 family. BCL-2 family members are known to be regulators of programmed cell death. This protein positively regulates cell apoptosis by forming heterodimers with BCL-xL and BCL-2, and reversing their death repressor activity. Proapoptotic activity of this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the regulation of this protein. Alternative splicing of this gene results in two transcript variants which encode the same isoform. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: BBC2; bcl-2 associated death agonist; bcl-2-binding component 6; bcl-2-like protein 8; BCL-X/BCL-2 binding protein; bcl-XL/Bcl-2-associated death promoter; bcl2 antagonist of cell death; BCL2-antagonist of cell death; BCL2-antagonist of cell death protein; BCL2-binding component 6; BCL2-binding protein; bcl2-L-8; BCL2L8; OTTHUMP00000165928; OTTHUMP00000165929
Orthologs: Mus musculus : Bad (BCL2-associated agonist of cell death)  MGI
Rattus norvegicus : Bad (BCL2-associated agonist of cell death)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11163,956,625 - 63,971,484-NCBI
Human Genome Assembly HuRef1160,365,093 - 60,379,900-NCBI
Human Genome Assembly GRCh371164,037,300 - 64,052,176-NCBI
Human Genome Assembly Build 361163,793,878 - 63,808,740-NCBI
Human Cytogenetic Map11q13.1 NCBI
Human Genome Assembly1163,793,877 - 63,808,740 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on BAD
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 735541
Created: 2004-02-06
Species: Homo sapiens
Last Modified: 2013-03-12
Status: ACTIVE