Human Gene SPI1 (uc001nfb.1)
  Description: Homo sapiens spleen focus forming virus (SFFV) proviral integration oncogene spi1 (SPI1), transcript variant 1, mRNA.
RefSeq Summary (NM_001080547): This gene encodes an ETS-domain transcription factor that activates gene expression during myeloid and B-lymphoid cell development. The nuclear protein binds to a purine-rich sequence known as the PU-box found near the promoters of target genes, and regulates their expression in coordination with other transcription factors and cofactors. The protein can also regulate alternative splicing of target genes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr11:47,376,409-47,400,127 Size: 23,719 Total Exon Count: 5 Strand: -
Coding Region
   Position: hg19 chr11:47,376,778-47,399,904 Size: 23,127 Coding Exon Count: 5 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr11:47,376,409-47,400,127)mRNA (may differ from genome)Protein (271 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkHGNCHPRDLynxMalacardsMGI
OMIMPubMedReactomeTreefamUniProtKBWikipedia
BioGrid CRISPR DB

-  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): SPI1
CDC HuGE Published Literature: SPI1

-  MalaCards Disease Associations
  MalaCards Gene Search: SPI1
Diseases sorted by gene-association score: neutrophil-specific granule deficiency (3), specific granule deficiency (3), poikiloderma with neutropenia (1), parotid gland cancer (1), leukemia, acute myeloid (1)

-  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: 439.24 RPKM in Whole Blood
Total median expression: 812.69 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.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -97.50223-0.437 Picture PostScript Text
3' UTR -133.51369-0.362 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:
PF00178 - Ets-domain

SCOP Domains:
46785 - "Winged helix" DNA-binding domain

ModBase Predicted Comparative 3D Structure on P17947-2
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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 orthologGenome BrowserGenome BrowserNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGDEnsembl   
 Protein SequenceProtein Sequence   
 AlignmentAlignment   

-  Descriptions from all associated GenBank mRNAs
  X52056 - Human mRNA for spi-1 proto-oncogene.
JD406318 - Sequence 387342 from Patent EP1572962.
JD523263 - Sequence 504287 from Patent EP1572962.
JD127040 - Sequence 108064 from Patent EP1572962.
JD405804 - Sequence 386828 from Patent EP1572962.
JD464430 - Sequence 445454 from Patent EP1572962.
JD405869 - Sequence 386893 from Patent EP1572962.
JD336189 - Sequence 317213 from Patent EP1572962.
BC111379 - Synthetic construct Homo sapiens clone IMAGE:40080653, MGC:133441 SPI1 protein (SPI1) mRNA, encodes complete protein.
AB464244 - Synthetic construct DNA, clone: pF1KB9697, Homo sapiens SPI1 gene for spleen focus forming virus (SFFV) proviral integration oncogene spi1, without stop codon, in Flexi system.
AK310065 - Homo sapiens cDNA, FLJ17107.
JD108790 - Sequence 89814 from Patent EP1572962.
JD468341 - Sequence 449365 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa05200 - Pathways in cancer
hsa05221 - Acute myeloid leukemia

Reactome (by CSHL, EBI, and GO)

Protein P17947 (Reactome details) participates in the following event(s):

R-HSA-8939236 RUNX1 regulates transcription of genes involved in differentiation of HSCs
R-HSA-8878171 Transcriptional regulation by RUNX1
R-HSA-212436 Generic Transcription Pathway
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-74160 Gene expression (Transcription)

-  Other Names for This Gene
  Alternate Gene Symbols: NM_001080547, NP_001074016, P17947-2
UCSC ID: uc001nfb.1
RefSeq Accession: NM_001080547
Protein: P17947-2, splice isoform of P17947 CCDS: CCDS7933.2, CCDS44591.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001080547.1
exon count: 5CDS single in 3' UTR: no RNA size: 1426
ORF size: 816CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1431.00frame shift in genome: no % Coverage: 98.74
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.