Human Gene BRD7 (uc002ege.2)
  Description: Homo sapiens bromodomain containing 7 (BRD7), transcript variant 1, mRNA.
RefSeq Summary (NM_001173984): This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010].
Transcript (Including UTRs)
   Position: hg19 chr16:50,352,929-50,402,845 Size: 49,917 Total Exon Count: 17 Strand: -
Coding Region
   Position: hg19 chr16:50,353,122-50,402,685 Size: 49,564 Coding Exon Count: 17 

Page IndexSequence and LinksPrimersGenetic AssociationsMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
mRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr16:50,352,929-50,402,845)mRNA (may differ from genome)Protein (652 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
H-INVHGNCLynxMalacardsMGIOMIM
PubMedReactomeTreefamUniProtKBWikipediaBioGrid 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


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): BRD7
CDC HuGE Published Literature: BRD7
Positive Disease Associations: Inflammatory Bowel Diseases
Related Studies:
  1. Inflammatory Bowel Diseases
    Richard H Duerr et al. Science (New York, N.Y.) 2006, A genome-wide association study identifies IL23R as an inflammatory bowel disease gene., Science (New York, N.Y.). [PubMed 17068223]
  2. Inflammatory Bowel Diseases
    Richard H Duerr et al. Science (New York, N.Y.) 2006, A genome-wide association study identifies IL23R as an inflammatory bowel disease gene., Science (New York, N.Y.). [PubMed 17068223]

-  MalaCards Disease Associations
  MalaCards Gene Search: BRD7
Diseases sorted by gene-association score: pharynx cancer (2)

-  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: 30.81 RPKM in Testis
Total median expression: 902.97 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 -117.30160-0.733 Picture PostScript Text
3' UTR -38.10193-0.197 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:
PF00439 - Bromodomain
PF12024 - Domain of unknown function (DUF3512)

SCOP Domains:
47370 - Bromodomain

ModBase Predicted Comparative 3D Structure on Q9NPI1-2
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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 orthologNo orthologNo orthologNo orthologGenome BrowserNo ortholog
Gene Details   Gene Details 
Gene Sorter   Gene Sorter 
    WormBase 
    Protein Sequence 
    Alignment 

-  Descriptions from all associated GenBank mRNAs
  AK074613 - Homo sapiens cDNA FLJ90132 fis, clone HEMBB1000542, highly similar to Mus musculus bromodomain-containing protein BP75 mRNA.
AF152604 - Homo sapiens bromodomain-containing protein (BRD7) mRNA, complete cds.
BC094706 - Homo sapiens bromodomain containing 7, mRNA (cDNA clone MGC:104375 IMAGE:30719813), complete cds.
AF213969 - Homo sapiens bromodomain protein CELTIX1 mRNA, complete cds.
JD566384 - Sequence 547408 from Patent EP1572962.
BC001611 - Homo sapiens, Similar to bromodomain-containing 7, clone IMAGE:3503011, mRNA, partial cds.
BC050728 - Homo sapiens bromodomain containing 7, mRNA (cDNA clone MGC:60365 IMAGE:6149862), complete cds.
AK027308 - Homo sapiens cDNA FLJ14402 fis, clone HEMBA1003783, moderately similar to Mus musculus bromodomain-containing protein BP75 mRNA.
AJ271881 - Homo sapiens mRNA for bromodomain containing protein (BP465 gene).
JD357319 - Sequence 338343 from Patent EP1572962.
AB527472 - Synthetic construct DNA, clone: pF1KB7890, Homo sapiens BRD7 gene for bromodomain containing 7, without stop codon, in Flexi system.
JD554194 - Sequence 535218 from Patent EP1572962.
DL490617 - Novel nucleic acids.
JD241183 - Sequence 222207 from Patent EP1572962.
JD039293 - Sequence 20317 from Patent EP1572962.
JD315629 - Sequence 296653 from Patent EP1572962.
JD315630 - Sequence 296654 from Patent EP1572962.
JD332858 - Sequence 313882 from Patent EP1572962.
JD445191 - Sequence 426215 from Patent EP1572962.
JD437765 - Sequence 418789 from Patent EP1572962.
JD177283 - Sequence 158307 from Patent EP1572962.
JD439341 - Sequence 420365 from Patent EP1572962.
JD382418 - Sequence 363442 from Patent EP1572962.
JD145051 - Sequence 126075 from Patent EP1572962.
JD038202 - Sequence 19226 from Patent EP1572962.
JD420736 - Sequence 401760 from Patent EP1572962.
JD522467 - Sequence 503491 from Patent EP1572962.
JD351483 - Sequence 332507 from Patent EP1572962.
JD384287 - Sequence 365311 from Patent EP1572962.
JD042417 - Sequence 23441 from Patent EP1572962.
JD050180 - Sequence 31204 from Patent EP1572962.
JD111895 - Sequence 92919 from Patent EP1572962.
JD141381 - Sequence 122405 from Patent EP1572962.
JD417090 - Sequence 398114 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q9NPI1 (Reactome details) participates in the following event(s):

R-HSA-3222093 BRD7 binds TP53 and EP300
R-HSA-5628871 BRD7 promotes EP300-mediated acetylation of TP53
R-HSA-6805650 MTA2-NuRD complex deacetylates TP53
R-HSA-6804758 Regulation of TP53 Activity through Acetylation
R-HSA-5633007 Regulation of TP53 Activity
R-HSA-3700989 Transcriptional Regulation by TP53
R-HSA-212436 Generic Transcription Pathway
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-74160 Gene expression (Transcription)

-  Other Names for This Gene
  Alternate Gene Symbols: BP75, CELTIX1, NM_001173984, NP_001167455, Q9NPI1-2
UCSC ID: uc002ege.2
RefSeq Accession: NM_001173984
Protein: Q9NPI1-2, splice isoform of Q9NPI1 CCDS: CCDS10742.1, CCDS54007.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001173984.2
exon count: 17CDS single in 3' UTR: no RNA size: 2330
ORF size: 1959CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 4118.00frame shift in genome: no % Coverage: 99.23
has start codon: yes stop codon in genome: no # of Alignments: 1
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.