Human Gene GCSAM (uc021xcl.1)
  Description: Homo sapiens germinal center-associated, signaling and motility (GCSAM), transcript variant 3, mRNA.
RefSeq Summary (NM_001190259): This gene encodes a protein which may function in signal transduction pathways and whose expression is elevated in germinal cell lymphomas. It contains a putative PDZ-interacting domain, an immunoreceptor tyrosine-based activation motif (ITAM), and two putative SH2 binding sites. In B cells, its expression is specifically induced by interleukin-4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr3:111,839,688-111,852,152 Size: 12,465 Total Exon Count: 6 Strand: -
Coding Region
   Position: hg19 chr3:111,842,302-111,851,967 Size: 9,666 Coding Exon Count: 6 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr3:111,839,688-111,852,152)mRNA (may differ from genome)Protein (180 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
H-INVHGNCLynxMalacardsMGIOMIM
PubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: C9JUG6_HUMAN
DESCRIPTION: SubName: Full=Germinal center-associated-signaling and motility protein;
CAUTION: The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.

-  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: GCSAM
Diseases sorted by gene-association score: lymphoma (9), diffuse large b-cell lymphoma (6)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  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: 53.15 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 89.58 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 -71.99185-0.389 Picture PostScript Text
3' UTR -700.032614-0.268 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:
PF15666 - Germinal center-associated lymphoma

ModBase Predicted Comparative 3D Structure on C9JUG6
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 orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Descriptions from all associated GenBank mRNAs
  AY212246 - Homo sapiens germinal center B-cell expressed transcript 2 (GCET2) mRNA, complete cds.
AF521911 - Homo sapiens HGAL mRNA, complete cds.
BC030506 - Homo sapiens germinal center expressed transcript 2, mRNA (cDNA clone MGC:40441 IMAGE:4385178), complete cds.
JD042972 - Sequence 23996 from Patent EP1572962.
JD180161 - Sequence 161185 from Patent EP1572962.
JD077396 - Sequence 58420 from Patent EP1572962.
JD049279 - Sequence 30303 from Patent EP1572962.
JD403771 - Sequence 384795 from Patent EP1572962.
JD049130 - Sequence 30154 from Patent EP1572962.
AK313368 - Homo sapiens cDNA, FLJ93897, highly similar to Homo sapiens germinal center expressed transcript 2 (GCET2), mRNA.
KJ900526 - Synthetic construct Homo sapiens clone ccsbBroadEn_09920 GCET2 gene, encodes complete protein.
HQ447219 - Synthetic construct Homo sapiens clone IMAGE:100070520; CCSB009605_01 germinal center expressed transcript 2 (GCET2) gene, encodes complete protein.
CU688884 - Synthetic construct Homo sapiens gateway clone IMAGE:100018155 5' read GCET2 mRNA.
AK128276 - Homo sapiens cDNA FLJ46413 fis, clone THYMU3011543.

-  Other Names for This Gene
  Alternate Gene Symbols: C9JUG6, C9JUG6_HUMAN, NM_001190259, NP_001177188
UCSC ID: uc021xcl.1
RefSeq Accession: NM_001190259
Protein: C9JUG6 CCDS: CCDS2964.1, CCDS54622.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001190259.1
exon count: 6CDS single in 3' UTR: no RNA size: 3355
ORF size: 543CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1283.00frame shift in genome: no % Coverage: 99.61
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.