Human Gene DISC2 (uc001hvd.3)
  Description: Homo sapiens disrupted in schizophrenia 2 (non-protein coding) (DISC2), non-coding RNA.
RefSeq Summary (NR_002227): DISC2 is thought to specify a noncoding RNA molecule antisense to DISC1 (MIM 605210). Both genes were found to be disrupted by a translocation in a large schizophrenia (MIM 181500) kindred.[supplied by OMIM, Jul 2002].
Transcript (Including UTRs)
   Position: hg19 chr1:231,950,372-231,954,263 Size: 3,892 Total Exon Count: 1 Strand: -


Page IndexSequence and LinksPrimersMalaCardsOther SpeciesmRNA Descriptions
Other NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:231,950,372-231,954,263)mRNA (may differ from genome)No protein
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaBioGPS
ExonPrimerGeneNetworkHGNCLynxMalacardsPubMed

-  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: DISC2
Diseases sorted by gene-association score: schizophrenia* (26)
* = Manually curated disease association

-  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
  JD063049 - Sequence 44073 from Patent EP1572962.
JD275692 - Sequence 256716 from Patent EP1572962.
JD111746 - Sequence 92770 from Patent EP1572962.
JD158839 - Sequence 139863 from Patent EP1572962.
JD111745 - Sequence 92769 from Patent EP1572962.
JD105606 - Sequence 86630 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: NR_002227
UCSC ID: uc001hvd.3
RefSeq Accession: NR_002227

-  Gene Model Information
 
category: antisense nonsense-mediated-decay: no RNA accession: NR_002227.2
exon count: 1CDS single in 3' UTR: no RNA size: 3892
ORF size: 0CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 407.50frame shift in genome: no % Coverage: 100.00
has start codon: no stop codon in genome: no # of Alignments: 1
has end codon: no 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.