Human Gene SLFN11 (uc010ctr.3)
  Description: Homo sapiens schlafen family member 11 (SLFN11), transcript variant 3, mRNA.
Transcript (Including UTRs)
   Position: hg19 chr17:33,677,329-33,700,720 Size: 23,392 Total Exon Count: 6 Strand: -
Coding Region
   Position: hg19 chr17:33,679,375-33,690,826 Size: 11,452 Coding Exon Count: 4 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr17:33,677,329-33,700,720)mRNA (may differ from genome)Protein (901 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsH-INV
HGNCHPRDLynxMalacardsMGIneXtProt
OMIMPubMedTreefamUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: SLN11_HUMAN
DESCRIPTION: RecName: Full=Schlafen family member 11;
FUNCTION: Interferon (IFN)-induced antiviral protein which acts as an inhibitor of retrovirus protein synthesis. Specifically abrogates the production of retroviruses such as human immunodeficiency virus 1 (HIV-1) by acting as a specific inhibitor of the synthesis of retroviruses encoded proteins in a codon- usage-dependent manner. Binds to tRNAs and exploits the unique viral codon bias towards A/T nucleotides. The exact inhibition mechanism is unclear: may either sequesters tRNAs, prevents their maturation via post-transcriptional processing or accelerates their deacylation. Does not inhibit reverse transcription, integration or production and nuclear export of viral RNA.
INDUCTION: By type I interferons, poly-IC and poly-dAdT.
SIMILARITY: Belongs to the Schlafen family.
SEQUENCE CAUTION: Sequence=BAB85010.1; Type=Frameshift; Positions=135;

-  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: SLFN11
Diseases sorted by gene-association score: ewing sarcoma (2)

-  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: 19.32 RPKM in Adipose - Visceral (Omentum)
Total median expression: 338.16 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 -151.40364-0.416 Picture PostScript Text
3' UTR -567.212046-0.277 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
  InterPro Domains: Graphical view of domain structure
IPR007421 - ATPase_AAA-4
IPR018647 - DUF2075

Pfam Domains:
PF04326 - Putative DNA-binding domain
PF09848 - Uncharacterized conserved protein (DUF2075)

SCOP Domains:
52540 - P-loop containing nucleoside triphosphate hydrolases

ModBase Predicted Comparative 3D Structure on Q7Z7L1
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     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000049 tRNA binding
GO:0000166 nucleotide binding
GO:0003723 RNA binding
GO:0004386 helicase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016787 hydrolase activity
GO:0016887 ATPase activity

Biological Process:
GO:0002376 immune system process
GO:0006974 cellular response to DNA damage stimulus
GO:0008156 negative regulation of DNA replication
GO:0010942 positive regulation of cell death
GO:0043111 replication fork arrest
GO:0051607 defense response to virus
GO:2000134 negative regulation of G1/S transition of mitotic cell cycle

Cellular Component:
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005694 chromosome
GO:0005829 cytosol
GO:0016235 aggresome


-  Descriptions from all associated GenBank mRNAs
  AK074184 - Homo sapiens mRNA for FLJ00257 protein.
AL831964 - Homo sapiens mRNA; cDNA DKFZp451E232 (from clone DKFZp451E232); complete cds.
BC052586 - Homo sapiens schlafen family member 11, mRNA (cDNA clone MGC:59997 IMAGE:6258140), complete cds.
AK092241 - Homo sapiens cDNA FLJ34922 fis, clone NT2RP7003084, weakly similar to Mus musculus schlafen3 (Slfn3) mRNA.
AX747425 - Sequence 950 from Patent EP1308459.
KJ904944 - Synthetic construct Homo sapiens clone ccsbBroadEn_14338 SLFN11-like gene, encodes complete protein.
AM393675 - Synthetic construct Homo sapiens clone IMAGE:100003079 for hypothetical protein (SLFN11 gene).
BC141660 - Synthetic construct Homo sapiens clone IMAGE:100002213, MGC:165129 schlafen family member 11 (SLFN11) mRNA, encodes complete protein.
AL512731 - Homo sapiens mRNA; cDNA DKFZp667B0711 (from clone DKFZp667B0711).
JD369285 - Sequence 350309 from Patent EP1572962.
JD188177 - Sequence 169201 from Patent EP1572962.
JD298702 - Sequence 279726 from Patent EP1572962.
JD521722 - Sequence 502746 from Patent EP1572962.
JD330360 - Sequence 311384 from Patent EP1572962.
JD410607 - Sequence 391631 from Patent EP1572962.
JD297114 - Sequence 278138 from Patent EP1572962.
JD163372 - Sequence 144396 from Patent EP1572962.
JD355868 - Sequence 336892 from Patent EP1572962.
JD343692 - Sequence 324716 from Patent EP1572962.
JD184704 - Sequence 165728 from Patent EP1572962.
JD561969 - Sequence 542993 from Patent EP1572962.
JD442411 - Sequence 423435 from Patent EP1572962.
JD386999 - Sequence 368023 from Patent EP1572962.
JD343077 - Sequence 324101 from Patent EP1572962.
JD349316 - Sequence 330340 from Patent EP1572962.
JD479209 - Sequence 460233 from Patent EP1572962.
JD551170 - Sequence 532194 from Patent EP1572962.
JD202041 - Sequence 183065 from Patent EP1572962.
JD171396 - Sequence 152420 from Patent EP1572962.
JD550936 - Sequence 531960 from Patent EP1572962.
AK310802 - Homo sapiens cDNA, FLJ17844.
JD162696 - Sequence 143720 from Patent EP1572962.
JD082669 - Sequence 63693 from Patent EP1572962.
JD082668 - Sequence 63692 from Patent EP1572962.
JD326093 - Sequence 307117 from Patent EP1572962.
JD439679 - Sequence 420703 from Patent EP1572962.
JD124269 - Sequence 105293 from Patent EP1572962.
JD540668 - Sequence 521692 from Patent EP1572962.
JD111236 - Sequence 92260 from Patent EP1572962.
JD423473 - Sequence 404497 from Patent EP1572962.
JD315647 - Sequence 296671 from Patent EP1572962.
LF327033 - JP 2014500723-A/134536: Polycomb-Associated Non-Coding RNAs.
JD522129 - Sequence 503153 from Patent EP1572962.
JD506691 - Sequence 487715 from Patent EP1572962.
JD429347 - Sequence 410371 from Patent EP1572962.
MA562610 - JP 2018138019-A/134536: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: E1P643, NM_001104589, NP_689483, Q7Z7L1, Q8N3S8, Q8N762, Q8TEE0, SLN11_HUMAN
UCSC ID: uc010ctr.3
RefSeq Accession: NM_001104589
Protein: Q7Z7L1 (aka SLN11_HUMAN)
CCDS: CCDS11294.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001104589.1
exon count: 6CDS single in 3' UTR: no RNA size: 5132
ORF size: 2706CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 5543.00frame shift in genome: no % Coverage: 99.69
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.