Human Gene BAG6 (uc003nvf.4)
  Description: Homo sapiens BCL2-associated athanogene 6 (BAG6), transcript variant 4, mRNA.
RefSeq Summary (NM_001098534): 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 addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr6:31,606,805-31,620,170 Size: 13,366 Total Exon Count: 25 Strand: -
Coding Region
   Position: hg19 chr6:31,606,908-31,619,540 Size: 12,633 Coding Exon Count: 24 

Page IndexSequence and LinksPrimersMalaCardsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesmRNA Descriptions
Other NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr6:31,606,805-31,620,170)mRNA (may differ from genome)Protein (1126 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCLynxMalacardsMGI
OMIMPubMedTreefamUniProtKBWikipediaBioGrid CRISPR DB

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: BAG6
Diseases sorted by gene-association score: acute diarrhea (11), discrete subaortic stenosis (9), primary amebic meningoencephalitis (9), subvalvular aortic stenosis (7), non-invasive bladder papillary urothelial neoplasm (6), gastroenteritis (5), coronary artery aneurysm (4), fructose-1,6-bisphosphatase deficiency (4), gastrointestinal system disease (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 146.61 RPKM in Testis
Total median expression: 2300.32 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -48.90160-0.306 Picture PostScript Text
3' UTR -19.40103-0.188 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  Pfam Domains:
PF00240 - Ubiquitin family
PF12057 - Domain of unknown function (DUF3538)
PF13881 - Ubiquitin-2 like Rad60 SUMO-like

SCOP Domains:
54236 - Ubiquitin-like

ModBase Predicted Comparative 3D Structure on P46379-2
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Descriptions from all associated GenBank mRNAs
  AK302695 - Homo sapiens cDNA FLJ60983 complete cds, highly similar to Large proline-rich protein BAT3.
BX647244 - Homo sapiens mRNA; cDNA DKFZp686L0653 (from clone DKFZp686L0653).
BC003133 - Homo sapiens HLA-B associated transcript 3, mRNA (cDNA clone MGC:3619 IMAGE:2957896), complete cds.
M33519 - Human HLA-B-associated transcript 3 (BAT3) mRNA, complete cds.
AK304879 - Homo sapiens cDNA FLJ61584 complete cds, highly similar to Large proline-rich protein BAT3.
KJ892447 - Synthetic construct Homo sapiens clone ccsbBroadEn_01841 BAG6 gene, encodes complete protein.
AB384971 - Synthetic construct DNA, clone: pF1KB4636, Homo sapiens BAT3 gene for large proline-rich protein BAT3, complete cds, without stop codon, in Flexi system.
JD027150 - Sequence 8174 from Patent EP1572962.
DQ591812 - Homo sapiens piRNA piR-58924, complete sequence.
CU678390 - Synthetic construct Homo sapiens gateway clone IMAGE:100020517 5' read BAT3 mRNA.
JD056311 - Sequence 37335 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: BAT3, G3, NM_001098534, NP_542434, P46379-2
UCSC ID: uc003nvf.4
RefSeq Accession: NM_001098534
Protein: P46379-2, splice isoform of P46379 CCDS: CCDS4709.1, CCDS47403.1, CCDS56415.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001098534.1
exon count: 25CDS single in 3' UTR: no RNA size: 3660
ORF size: 3381CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 4994.00frame shift in genome: no % Coverage: 99.56
has start codon: yes stop codon in genome: no # of Alignments: 7
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.