Human Gene YTHDF3 (uc003xuz.4)
  Description: Homo sapiens YTH domain family, member 3 (YTHDF3), transcript variant 6, mRNA.
RefSeq Summary (NM_001277817): This gene encodes a member of the YTH (YT521-B homology) domain protein family. The YTH domain is common in eukaryotes, is often found in the middle of the protein sequence, and may function in binding to RNA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013].
Transcript (Including UTRs)
   Position: hg19 chr8:64,081,186-64,125,346 Size: 44,161 Total Exon Count: 5 Strand: +
Coding Region
   Position: hg19 chr8:64,098,732-64,122,264 Size: 23,533 Coding Exon Count: 2 

Page IndexSequence and LinksUniProtKB CommentsPrimersGenetic AssociationsCTD
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 (chr8:64,081,186-64,125,346)mRNA (may differ from genome)Protein (534 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
H-INVHGNCHPRDLynxMGIneXtProt
OMIMPubMedUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: YTHD3_HUMAN
DESCRIPTION: RecName: Full=YTH domain family protein 3;
INTERACTION: P04591:gag (xeno); NbExp=2; IntAct=EBI-2849837, EBI-6179727;
SIMILARITY: Contains 1 YTH domain.

-  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): YTHDF3
CDC HuGE Published Literature: YTHDF3
Positive Disease Associations: Cholesterol, LDL , Erythrocytes , Magnesium , Stroke
Related Studies:
  1. Cholesterol, LDL
    Sekar Kathiresan et al. BMC medical genetics 2007, A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study., BMC medical genetics. [PubMed 17903299]
    Using a 100K genome-wide scan, we have generated a set of putative associations for common sequence variants and lipid phenotypes. Validation of selected hypotheses in additional samples did not identify any new loci underlying variability in blood lipids. Lack of replication may be due to inadequate statistical power to detect modest quantitative trait locus effects (i.e., <1% of trait variance explained) or reduced genomic coverage of the 100K array. GWAS in FHS using a denser genome-wide genotyping platform and a better-powered replication strategy may identify novel loci underlying blood lipids.
  2. Erythrocytes
    , , . [PubMed 0]
  3. Erythrocytes
    , , . [PubMed 0]
           more ... click here to view the complete list

-  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: 18.39 RPKM in Cells - Cultured fibroblasts
Total median expression: 520.98 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 -107.69325-0.331 Picture PostScript Text
3' UTR -762.423082-0.247 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
IPR007275 - YTH_domain

Pfam Domains:
PF04146 - YT521-B-like domain

ModBase Predicted Comparative 3D Structure on Q7Z739
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:0003723 RNA binding
GO:0005515 protein binding
GO:0043022 ribosome binding
GO:1990247 N6-methyladenosine-containing RNA binding

Biological Process:
GO:0045727 positive regulation of translation
GO:0045948 positive regulation of translational initiation
GO:0061157 mRNA destabilization

Cellular Component:
GO:0005737 cytoplasm
GO:0005829 cytosol


-  Descriptions from all associated GenBank mRNAs
  BC052970 - Homo sapiens YTH domain family, member 3, mRNA (cDNA clone MGC:54324 IMAGE:6044054), complete cds.
AK127574 - Homo sapiens cDNA FLJ45669 fis, clone CTONG3003669, highly similar to YTH domain protein 3.
AL832005 - Homo sapiens mRNA; cDNA DKFZp451O193 (from clone DKFZp451O193).
BX537996 - Homo sapiens mRNA; cDNA DKFZp451M1911 (from clone DKFZp451M1911).
AL831816 - Homo sapiens mRNA; cDNA DKFZp451A052 (from clone DKFZp451A052).
AK056219 - Homo sapiens cDNA FLJ31657 fis, clone NT2RI2004304, moderately similar to Homo sapiens NY-REN-2 antigen mRNA.
BC037492 - Homo sapiens cDNA clone IMAGE:5260578, containing frame-shift errors.
AL832335 - Homo sapiens mRNA; cDNA DKFZp451J085 (from clone DKFZp451J085).
CU690942 - Synthetic construct Homo sapiens gateway clone IMAGE:100021491 5' read YTHDF3 mRNA.
AB463357 - Synthetic construct DNA, clone: pF1KB8698, Homo sapiens YTHDF3 gene for YTH domain family, member 3, without stop codon, in Flexi system.
AM393482 - Synthetic construct Homo sapiens clone IMAGE:100002145 for hypothetical protein (YTHDF3 gene).
AM393861 - Synthetic construct Homo sapiens clone IMAGE:100002144 for hypothetical protein (YTHDF3 gene).
KJ895899 - Synthetic construct Homo sapiens clone ccsbBroadEn_05293 YTHDF3 gene, encodes complete protein.
AK093081 - Homo sapiens cDNA FLJ35762 fis, clone TESTI2004793, moderately similar to Homo sapiens NY-REN-2 antigen mRNA.
AX747908 - Sequence 1433 from Patent EP1308459.
AK298544 - Homo sapiens cDNA FLJ56221 complete cds, highly similar to YTH domain protein 3.
AL832369 - Homo sapiens mRNA; cDNA DKFZp451B107 (from clone DKFZp451B107).
JD093132 - Sequence 74156 from Patent EP1572962.
JD282567 - Sequence 263591 from Patent EP1572962.
JD470562 - Sequence 451586 from Patent EP1572962.
JD391617 - Sequence 372641 from Patent EP1572962.
JD440484 - Sequence 421508 from Patent EP1572962.
JD460707 - Sequence 441731 from Patent EP1572962.
JD503944 - Sequence 484968 from Patent EP1572962.
JD552420 - Sequence 533444 from Patent EP1572962.
JD514584 - Sequence 495608 from Patent EP1572962.
JD290005 - Sequence 271029 from Patent EP1572962.
AK002173 - Homo sapiens cDNA FLJ11311 fis, clone PLACE1010102.
AL050081 - Homo sapiens mRNA; cDNA DKFZp566J2146 (from clone DKFZp566J2146).

-  Other Names for This Gene
  Alternate Gene Symbols: B3KXL4, NM_001277817, NP_001264746, Q63Z37, Q659A3, Q7Z739, uc003xuz.3, YTHD3_HUMAN
UCSC ID: uc003xuz.4
RefSeq Accession: NM_001277817
Protein: Q7Z739 (aka YTHD3_HUMAN)

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001277817.1
exon count: 5CDS single in 3' UTR: no RNA size: 5010
ORF size: 1596CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 2758.50frame shift in genome: no % Coverage: 99.86
has start codon: no 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.