Human Gene BLCAP (uc002xhc.1)
  Description: bladder cancer associated protein
RefSeq Summary (NM_006698): This gene encodes a protein that reduces cell growth by stimulating apoptosis. Alternative splicing and the use of alternative promoters result in multiple transcript variants encoding the same protein. This gene is imprinted in brain where different transcript variants are expressed from each parental allele. Transcript variants initiating from the upstream promoter are expressed preferentially from the maternal allele, while transcript variants initiating downstream of the interspersed NNAT gene (GeneID:4826) are expressed from the paternal allele. Transcripts at this locus may also undergo A to I editing, resulting in amino acid changes at three positions in the N-terminus of the protein. [provided by RefSeq, Nov 2015].
Transcript (Including UTRs)
   Position: hg18 chr20:35,579,233-35,589,717 Size: 10,485 Total Exon Count: 2 Strand: -
Coding Region
   Position: hg18 chr20:35,580,727-35,580,990 Size: 264 Coding Exon Count: 1 

Page IndexSequence and LinksUniProtKB CommentsPrimersCTDMicroarray Expression
RNA StructureProtein StructureOther SpeciesGO AnnotationsmRNA DescriptionsOther Names
Model InformationMethods
Data last updated at UCSC: 2009-03-03

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr20:35,579,233-35,589,717)mRNA (may differ from genome)Protein (87 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCHPRDMGIOMIM
PubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: BLCAP_HUMAN
DESCRIPTION: RecName: Full=Bladder cancer-associated protein; AltName: Full=Bladder cancer 10 kDa protein; Short=Bc10;
FUNCTION: May regulate cell proliferation and coordinate apoptosis and cell cycle progression via a novel mechanism independent of both p53/TP53 and NF-kappa-B.
INTERACTION: P03372:ESR1; NbExp=2; IntAct=EBI-3895726, EBI-78473;
SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein (Potential).
TISSUE SPECIFICITY: Expressed in cervical tissues. Down-regulated during bladder cancer progression and in most cervical carcinomas.
SIMILARITY: Belongs to the BLCAP family.
WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and Haematology; URL="http://atlasgeneticsoncology.org/Genes/BLCAPID801ch20q11.html";

-  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


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

-  Microarray Expression Data
 
Expression ratio colors:

GNF Expression Atlas 2 Data from U133A and GNF1H Chips

      
      
      
     
    
     
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Affymetrix All Exon Microarrays

           
Ratios

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -131.90285-0.463 Picture PostScript Text
3' UTR -512.501494-0.343 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
  InterPro Domains: Graphical view of domain structure
IPR009598 - BC10
IPR018015 - BC10-like

Pfam Domains:
PF06726 - Bladder cancer-related protein BC10

ModBase Predicted Comparative 3D Structure on P62952
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
Genome BrowserNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
MGIRGD    
Protein Sequence     
Alignment     

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding

Biological Process:
GO:0006915 apoptotic process
GO:0007049 cell cycle
GO:0030262 apoptotic nuclear changes

Cellular Component:
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  BC071704 - Homo sapiens bladder cancer associated protein, mRNA (cDNA clone MGC:87985 IMAGE:5190373), complete cds.
AF053470 - Homo sapiens 10kD protein (BC10) mRNA, complete cds.
BC047692 - Homo sapiens bladder cancer associated protein, mRNA (cDNA clone MGC:51898 IMAGE:6059195), complete cds.
AK124822 - Homo sapiens cDNA FLJ42832 fis, clone BRCAN2018748, highly similar to Bladder cancer-associated protein.
AK074498 - Homo sapiens cDNA FLJ90017 fis, clone HEMBA1000713, highly similar to Homo sapiens 10kD protein (BC10) mRNA.
AL049288 - Homo sapiens mRNA; cDNA DKFZp564M053 (from clone DKFZp564M053).
BC001481 - Homo sapiens ferritin, heavy polypeptide 1, mRNA (cDNA clone IMAGE:2966857), **** WARNING: chimeric clone ****.
JD525957 - Sequence 506981 from Patent EP1572962.
JD351277 - Sequence 332301 from Patent EP1572962.
JD488530 - Sequence 469554 from Patent EP1572962.
JD492366 - Sequence 473390 from Patent EP1572962.
JD371767 - Sequence 352791 from Patent EP1572962.
JD500648 - Sequence 481672 from Patent EP1572962.
JD565087 - Sequence 546111 from Patent EP1572962.
JD494138 - Sequence 475162 from Patent EP1572962.
JD409611 - Sequence 390635 from Patent EP1572962.
JD463455 - Sequence 444479 from Patent EP1572962.
KJ893159 - Synthetic construct Homo sapiens clone ccsbBroadEn_02553 BLCAP gene, encodes complete protein.
HQ257898 - Synthetic construct Homo sapiens clone IMAGE:100072207 Unknown protein gene, encodes complete protein.
JD329762 - Sequence 310786 from Patent EP1572962.
JD329761 - Sequence 310785 from Patent EP1572962.
JD338614 - Sequence 319638 from Patent EP1572962.
JD293830 - Sequence 274854 from Patent EP1572962.
JD154130 - Sequence 135154 from Patent EP1572962.
JD175165 - Sequence 156189 from Patent EP1572962.
JD330454 - Sequence 311478 from Patent EP1572962.
JD077131 - Sequence 58155 from Patent EP1572962.
JD260701 - Sequence 241725 from Patent EP1572962.
JD300723 - Sequence 281747 from Patent EP1572962.
JD318400 - Sequence 299424 from Patent EP1572962.
JD232076 - Sequence 213100 from Patent EP1572962.
JD254791 - Sequence 235815 from Patent EP1572962.
JD297368 - Sequence 278392 from Patent EP1572962.
JD142702 - Sequence 123726 from Patent EP1572962.
JD221032 - Sequence 202056 from Patent EP1572962.
LF205203 - JP 2014500723-A/12706: Polycomb-Associated Non-Coding RNAs.
LF317693 - JP 2014500723-A/125196: Polycomb-Associated Non-Coding RNAs.
MA440780 - JP 2018138019-A/12706: Polycomb-Associated Non-Coding RNAs.
MA553270 - JP 2018138019-A/125196: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: A2A2K7, BC10, BLCAP_HUMAN, NM_006698, NP_006689, O60629, P62952, Q9D3B5
UCSC ID: uc002xhc.1
RefSeq Accession: NM_006698
Protein: P62952 (aka BLCAP_HUMAN)
CCDS: CCDS13295.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_006698.2
exon count: 2CDS single in 3' UTR: no RNA size: 2057
ORF size: 264CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 692.00frame shift in genome: no % Coverage: 99.32
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.