Gene Gene information from NCBI Gene database.
Entrez ID 7917
Gene name BAG cochaperone 6
Gene symbol BAG6
Synonyms (NCBI Gene)
BAG-6BAT3D6S52EG3
Chromosome 6
Chromosome location 6p21.33
Summary This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In
miRNA miRNA information provided by mirtarbase database.
31
miRTarBase ID miRNA Experiments Reference
MIRT025262 hsa-miR-34a-5p Proteomics 21566225
MIRT025262 hsa-miR-34a-5p Proteomics 21566225
MIRT031479 hsa-miR-16-5p Proteomics 18668040
MIRT051911 hsa-let-7b-5p CLASH 23622248
MIRT049283 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
80
GO ID Ontology Definition Evidence Reference
GO:0001822 Process Kidney development IEA
GO:0001822 Process Kidney development ISS
GO:0002376 Process Immune system process IEA
GO:0002429 Process Immune response-activating cell surface receptor signaling pathway IDA 18852879
GO:0005102 Function Signaling receptor binding IPI 18852879
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
142590 13919 ENSG00000204463
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P46379
Protein name Large proline-rich protein BAG6 (BAG family molecular chaperone regulator 6) (BCL2-associated athanogene 6) (BAG-6) (HLA-B-associated transcript 3) (Protein G3) (Protein Scythe)
Protein function ATP-independent molecular chaperone preventing the aggregation of misfolded and hydrophobic patches-containing proteins (PubMed:21636303). Functions as part of a cytosolic protein quality control complex, the BAG6/BAT3 complex, which maintains t
PDB 1WX9 , 2N9P , 4DWF , 4EEW , 4WWR , 4X86 , 6AU8 , 7RU9 , 7RUA , 7RUC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00240 ubiquitin 19 89 Ubiquitin family Domain
PF12057 BAG6 276 392 BCL2-associated athanogene 6 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed by immature dendritic cells (at protein level). {ECO:0000269|PubMed:18852879}.
Sequence
MEPNDSTSTAVEEPDSLEVLVKTLDSQTRTFIVGAQMNVKEFKEHIAASVSIPSEKQRLI
YQGRVLQDDKKLQEYNVGGKVIHLVERAP
PQTHLPSGASSGTGSASATHGGGSPPGTRGP
GASVHDRNANSYVMVGTFNLPSDGSAVDVHINMEQAPIQSEPRVRLVMAQHMIRDIQTLL
SRMETLPYLQCRGGPQPQHSQPPPQPPAVTPEPVALSSQTSEPVESEAPPREPMEAEEVE
ERAPAQNPELTPGPAPAGPTPAPETNAPNHPSPAEYVEVLQELQRLESRLQPFLQRYYEV
LGAAATTDYNNNHEGREEDQRLINLVGESLRLLGNTFVALSDLRCNLACTPPRHLHVVRP
MSHYTTPMVLQQAAIPIQINVGTTVTMTGNGT
RPPPTPNAEAPPPGPGQASSVAPSSTNV
ESSAEGAPPPGPAPPPATSHPRVIRISHQSVEPVVMMHMNIQDSGTQPGGVPSAPTGPLG
PPGHGQTLGQQVPGFPTAPTRVVIARPTPPQARPSHPGGPPVSGTLQGAGLGTNASLAQM
VSGLVGQLLMQPVLVAQGTPGMAPPPAPATASASAGTTNTATTAGPAPGGPAQPPPTPQP
SMADLQFSQLLGNLLGPAGPGAGGSGVASPTITVAMPGVPAFLQGMTDFLQATQTAPPPP
PPPPPPPPAPEQQTMPPPGSPSGGAGSPGGLGLESLSPEFFTSVVQGVLSSLLGSLGARA
GSSESIAAFIQRLSGSSNIFEPGADGALGFFGALLSLLCQNFSMVDVVMLLHGHFQPLQR
LQPQLRSFFHQHYLGGQEPTPSNIRMATHTLITGLEEYVRESFSLVQVQPGVDIIRTNLE
FLQEQFNSIAAHVLHCTDSGFGARLLELCNQGLFECLALNLHCLGGQQMELAAVINGRIR
RMSRGVNPSLVSWLTTMMGLRLQVVLEHMPVGPDAILRYVRRVGDPPQPLPEEPMEVQGA
ERASPEPQRENASPAPGTTAEEAMSRGPPPAPEGGSRDEQDGASAETEPWAAAVPPEWVP
IIQQDIQSQRKVKPQPPLSDAYLSGMPAKRRKTMQGEGPQLLLSEAVSRAAKAAGARPLT
SPESLSRDLEAPEVQESYRQQLRSDIQKRLQEDPNYSPQRFPNAQRAFADDP
Sequence length 1132
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Protein export  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
6
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cerebellar vermis hypoplasia Uncertain significance rs1281308977 RCV001257950
Isolated unilateral hemispheric cerebellar hypoplasia Uncertain significance rs1281308977 RCV000779631
Nonpapillary renal cell carcinoma Uncertain significance rs374964997 RCV005927446
Ovarian serous cystadenocarcinoma Uncertain significance rs374964997 RCV005927447
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 39201500
Anxiety Disorders Associate 34741163
Ataxia Telangiectasia Associate 37296624
Carcinoma Hepatocellular Associate 29706626
Carcinoma Non Small Cell Lung Associate 25884493
Carcinoma Squamous Cell Associate 35499292
Coronary Aneurysm Associate 20626023
Coronary Artery Disease Associate 39201500
Diabetes Mellitus Type 2 Associate 27515906
Epilepsy Associate 24861996