Human Gene SNORD38B (uc001cml.3)
  Description: Homo sapiens small nucleolar RNA, C/D box 38B (SNORD38B), small nucleolar RNA.
Transcript (Including UTRs)
   Position: hg19 chr1:45,244,062-45,244,130 Size: 69 Total Exon Count: 1 Strand: +


Page IndexSequence and LinksPrimersCTDRNA-Seq ExpressionMicroarray Expression
Other SpeciesmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:45,244,062-45,244,130)mRNA (may differ from genome)No protein
Gene SorterGenome BrowserOther Species FASTATable SchemaBioGPSEnsembl
ExonPrimerGeneNetworkHGNCLynxPubMed

-  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

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 0.00 RPKM in Adipose - Subcutaneous
Total median expression: 0.00 RPKM



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

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  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
  LP896813 - Sequence 1677 from Patent EP3253886.
X97583 - H.sapiens small nucleolar RNA U38b.
HI965624 - Sequence 909 from Patent WO2010139812.
JA401662 - Sequence 909 from Patent WO2011080318.
JA402640 - Sequence 909 from Patent WO2011080315.
JA403647 - Sequence 909 from Patent WO2011080316.
JA406278 - Sequence 909 from Patent EP2336353.
JA429804 - Sequence 909 from Patent WO2011095623.
MS834763 - Sequence 909 from Patent EP3112479.
JC506923 - Sequence 291 from Patent EP2733220.
JC738035 - Sequence 291 from Patent WO2014075939.
DQ571419 - Homo sapiens piRNA piR-31531, complete sequence.
LQ980361 - Sequence 7 from Patent WO2013050532.

-  Other Names for This Gene
  Alternate Gene Symbols: NR_001457
UCSC ID: uc001cml.3
RefSeq Accession: NR_001457

-  Gene Model Information
 
category: noncoding nonsense-mediated-decay: no RNA accession: NR_001457.1
exon count: 1CDS single in 3' UTR: no RNA size: 69
ORF size: 0CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 278.00frame 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.