Human Gene TBATA (uc001jrj.1)
  Description: Homo sapiens thymus, brain and testes associated (TBATA), mRNA.
RefSeq Summary (NM_152710): This gene encodes a protein that regulates thymic epithelial cell proliferation and thymus size. It has been identified as a ligand for the class I human leukocyte antigen (HLA-I) in thymus. Studies of the orthologous mouse protein suggest that it may also play a role in spermatid differentiation, as well as in neuronal morphogenesis and synaptic plasticity. Polymorphisms in this gene are associated with susceptibility for multiple sclerosis (MS). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015].
Transcript (Including UTRs)
   Position: hg19 chr10:72,530,995-72,545,157 Size: 14,163 Total Exon Count: 11 Strand: -
Coding Region
   Position: hg19 chr10:72,531,132-72,543,135 Size: 12,004 Coding Exon Count: 9 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr10:72,530,995-72,545,157)mRNA (may differ from genome)Protein (351 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
H-INVHGNCHPRDLynxMalacardsMGI
neXtProtOMIMPubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: TBATA_HUMAN
DESCRIPTION: RecName: Full=Protein TBATA; AltName: Full=Protein SPATIAL; AltName: Full=Stromal protein associated with thymii and lymph node homolog; AltName: Full=Thymus, brain and testes-associated protein;
FUNCTION: May play a role in spermatid differentiation (By similarity). Modulates thymic stromal cell proliferation and thymus function (By similarity).
SUBCELLULAR LOCATION: Cytoplasm, cytosol (By similarity).
SIMILARITY: Belongs to the TBATA family.

-  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: TBATA
Diseases sorted by gene-association score: neurotic disorder (5)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene
  • C028474 1,4-bis(2-(3,5-dichloropyridyloxy))benzene
  • D018817 N-Methyl-3,4-methylenedioxyamphetamine
  • D013749 Tetrachlorodibenzodioxin
  • C069837 fullerene C60
  • C028007 nickel monoxide

+  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: 22.20 RPKM in Testis
Total median expression: 23.40 RPKM



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

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -103.56390-0.266 Picture PostScript Text
3' UTR -30.20137-0.220 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:
PF15256 - SPATIAL

ModBase Predicted Comparative 3D Structure on Q96M53
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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 orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Biological Process:
GO:0007275 multicellular organism development
GO:0007283 spermatogenesis
GO:0030154 cell differentiation

Cellular Component:
GO:0005737 cytoplasm
GO:0005829 cytosol


-  Descriptions from all associated GenBank mRNAs
  AK124147 - Homo sapiens cDNA FLJ42153 fis, clone THYMU2003397.
AK057382 - Homo sapiens cDNA FLJ32820 fis, clone TESTI2002965.
BC060774 - Homo sapiens cDNA clone IMAGE:5297282, with apparent retained intron.
BC139728 - Homo sapiens chromosome 10 open reading frame 27, mRNA (cDNA clone MGC:133265 IMAGE:40036949), complete cds.
JD489380 - Sequence 470404 from Patent EP1572962.
BC137543 - Homo sapiens chromosome 10 open reading frame 27, mRNA (cDNA clone MGC:169166 IMAGE:9021543), complete cds.
BC137544 - Homo sapiens chromosome 10 open reading frame 27, mRNA (cDNA clone MGC:169167 IMAGE:9021544), complete cds.
BC144692 - Homo sapiens chromosome 10 open reading frame 27, mRNA (cDNA clone MGC:178243 IMAGE:9053226), complete cds.
BC144694 - Homo sapiens chromosome 10 open reading frame 27, mRNA (cDNA clone MGC:178245 IMAGE:9053228), complete cds.
BC144695 - Homo sapiens cDNA clone IMAGE:9053229, containing frame-shift errors.
JD072487 - Sequence 53511 from Patent EP1572962.
KJ895835 - Synthetic construct Homo sapiens clone ccsbBroadEn_05229 C10orf27 gene, encodes complete protein.
AK310732 - Homo sapiens cDNA, FLJ17774.
AK303344 - Homo sapiens cDNA FLJ58964 complete cds.
AK303242 - Homo sapiens cDNA FLJ57695 complete cds.
AK310699 - Homo sapiens cDNA, FLJ17741.
AK303491 - Homo sapiens cDNA FLJ58894 complete cds.
JD054006 - Sequence 35030 from Patent EP1572962.
JD462375 - Sequence 443399 from Patent EP1572962.
JD307479 - Sequence 288503 from Patent EP1572962.
JD491296 - Sequence 472320 from Patent EP1572962.
JD111662 - Sequence 92686 from Patent EP1572962.
JD385422 - Sequence 366446 from Patent EP1572962.
JD090225 - Sequence 71249 from Patent EP1572962.
JD443095 - Sequence 424119 from Patent EP1572962.
JD490354 - Sequence 471378 from Patent EP1572962.
JD133491 - Sequence 114515 from Patent EP1572962.
JD295981 - Sequence 277005 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: A4QPA8, B2RPQ2, C10orf27, NM_152710, NP_689923, Q5T4G2, Q96M53, SPATIAL, TBATA_HUMAN
UCSC ID: uc001jrj.1
RefSeq Accession: NM_152710
Protein: Q96M53 (aka TBATA_HUMAN)
CCDS: CCDS7308.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_152710.2
exon count: 11CDS single in 3' UTR: no RNA size: 1583
ORF size: 1056CDS single in intron: no Alignment % ID: 99.94
txCdsPredict score: 2286.50frame shift in genome: no % Coverage: 100.00
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.