Human Gene RBMS2 (uc009zou.2)
  Description: Homo sapiens RNA binding motif, single stranded interacting protein 2 (RBMS2), mRNA.
RefSeq Summary (NM_002898): The protein encoded by this gene is a member of a small family of proteins which bind single stranded DNA/RNA. These proteins are characterized by the presence of two sets of ribonucleoprotein consensus sequence (RNP-CS) that contain conserved motifs, RNP1 and RNP2, originally described in RNA binding proteins, and required for DNA binding. The RBMS proteins have been implicated in such diverse functions as DNA replication, gene transcription, cell cycle progression and apoptosis. This protein was isolated by phenotypic complementation of cdc2 and cdc13 mutants of yeast and is thought to suppress cdc2 and cdc13 mutants through the induction of translation of cdc2. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr12:56,915,609-56,989,980 Size: 74,372 Total Exon Count: 12 Strand: +
Coding Region
   Position: hg19 chr12:56,975,290-56,983,045 Size: 7,756 Coding Exon Count: 8 

Page IndexSequence and LinksPrimersGenetic AssociationsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureOther SpeciesmRNA DescriptionsOther Names
Model InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr12:56,915,609-56,989,980)mRNA (may differ from genome)Protein (205 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaBioGPS
EnsemblExonPrimerGeneCardsGeneNetworkH-INVHGNC
LynxMGIPubMedTreefam

-  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): RBMS2
CDC HuGE Published Literature: RBMS2
Positive Disease Associations: Adiponectin , Amyotrophic Lateral Sclerosis
Related Studies:
  1. Adiponectin
    Zari Dastani et al. PLoS genetics 2012, Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals., PLoS genetics. [PubMed 22479202]
  2. Amyotrophic Lateral Sclerosis
    Jennifer C Schymick et al. Lancet neurology 2007, Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data., Lancet neurology. [PubMed 17362836]
    We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.

-  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: 18.03 RPKM in Lung
Total median expression: 248.52 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 -205.83789-0.261 Picture PostScript Text
3' UTR -2301.776935-0.332 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.

-  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
      
      
      
      
      

-  Descriptions from all associated GenBank mRNAs
  BC072679 - Homo sapiens RNA binding motif, single stranded interacting protein 2, mRNA (cDNA clone MGC:88016 IMAGE:6048623), complete cds.
AK308885 - Homo sapiens cDNA, FLJ98926.
AK304540 - Homo sapiens cDNA FLJ50371 complete cds, highly similar to RNA-binding motif,single-stranded-interacting protein 2.
AK293315 - Homo sapiens cDNA FLJ60228 complete cds, highly similar to RNA-binding motif, single-stranded-interacting protein 2.
JD503520 - Sequence 484544 from Patent EP1572962.
D28483 - Homo sapiens scr3 mRNA for RNA binding protein SCR3, complete cds.
AK299580 - Homo sapiens cDNA FLJ53090 complete cds, moderately similar to RNA-binding motif, single-stranded-interacting protein 2.
BC027863 - Homo sapiens RNA binding motif, single stranded interacting protein 2, mRNA (cDNA clone MGC:34559 IMAGE:5202634), complete cds.
CU693300 - Synthetic construct Homo sapiens gateway clone IMAGE:100019266 5' read RBMS2 mRNA.
KJ897455 - Synthetic construct Homo sapiens clone ccsbBroadEn_06849 RBMS2 gene, encodes complete protein.
JD296834 - Sequence 277858 from Patent EP1572962.
JD286111 - Sequence 267135 from Patent EP1572962.
GU228575 - Homo sapiens LSINCT3 non-coding RNA, partial sequence.
AK125252 - Homo sapiens cDNA FLJ43262 fis, clone HLUNG2003003.
JD415699 - Sequence 396723 from Patent EP1572962.
AK097342 - Homo sapiens cDNA FLJ40023 fis, clone STOMA2007680.
JD513904 - Sequence 494928 from Patent EP1572962.
JD120533 - Sequence 101557 from Patent EP1572962.
AK096412 - Homo sapiens cDNA FLJ39093 fis, clone NT2RP7020112.

-  Other Names for This Gene
  Alternate Gene Symbols: AK308885
UCSC ID: uc009zou.2
RefSeq Accession: NM_002898

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: AK308885.1
exon count: 12CDS single in 3' UTR: no RNA size: 1633
ORF size: 618CDS single in intron: no Alignment % ID: 99.76
txCdsPredict score: 907.00frame 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.