Human Gene HDGFL1 (uc003nds.3)
  Description: Homo sapiens hepatoma derived growth factor-like 1 (HDGFL1), mRNA.
Transcript (Including UTRs)
   Position: hg19 chr6:22,569,678-22,570,750 Size: 1,073 Total Exon Count: 1 Strand: +
Coding Region
   Position: hg19 chr6:22,569,805-22,570,560 Size: 756 Coding Exon Count: 1 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr6:22,569,678-22,570,750)mRNA (may differ from genome)Protein (251 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
HGNCHPRDLynxMGIneXtProtPubMed
TreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: HDGL1_HUMAN
DESCRIPTION: RecName: Full=Hepatoma-derived growth factor-like protein 1; AltName: Full=PWWP domain-containing protein 1;
SIMILARITY: Belongs to the HDGF family.
SIMILARITY: Contains 1 PWWP 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): HDGFL1
CDC HuGE Published Literature: HDGFL1
Positive Disease Associations: Bone Density , Carotid Artery Diseases , CD40 Ligand , Cholesterol, HDL , Hemoglobin A, Glycosylated , Platelet Aggregation , Stroke
Related Studies:
  1. Bone Density
    Douglas P Kiel et al. BMC medical genetics 2007, Genome-wide association with bone mass and geometry in the Framingham Heart Study., BMC medical genetics. [PubMed 17903296]
    The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.
  2. Carotid Artery Diseases
    Christopher J O'Donnell et al. BMC medical genetics 2007, Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study., BMC medical genetics. [PubMed 17903303]
    The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.
  3. CD40 Ligand
    Emelia J Benjamin et al. BMC medical genetics 2007, Genome-wide association with select biomarker traits in the Framingham Heart Study., BMC medical genetics. [PubMed 17903293]
    The Framingham GWAS represents a resource to describe potentially novel genetic influences on systemic biomarker variability. The newly described associations will need to be replicated in other studies.
           more ... click here to view the complete list

-  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: 102.49 RPKM in Testis
Total median expression: 103.08 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 -44.00127-0.346 Picture PostScript Text
3' UTR -58.40190-0.307 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
IPR000313 - PWWP

Pfam Domains:
PF00855 - PWWP domain

SCOP Domains:
63748 - Tudor/PWWP/MBT

ModBase Predicted Comparative 3D Structure on Q5TGJ6
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
      
      
      
      
      

-  Descriptions from all associated GenBank mRNAs
  HM005397 - Homo sapiens clone HTL-T-84 testicular tissue protein Li 84 mRNA, complete cds.
AK302110 - Homo sapiens cDNA FLJ50911 complete cds, moderately similar to Homo sapiens hepatoma derived growth factor-like 1 (HDGFL1), mRNA.
AK056824 - Homo sapiens cDNA FLJ32262 fis, clone PROST1000362, moderately similar to HEPATOMA-DERIVED GROWTH FACTOR.
BC172324 - Synthetic construct Homo sapiens clone IMAGE:100069018, MGC:199029 hepatoma derived growth factor-like 1 (HDGFL1) mRNA, encodes complete protein.
DQ584678 - Homo sapiens piRNA piR-51790, complete sequence.
JD137638 - Sequence 118662 from Patent EP1572962.
JD229293 - Sequence 210317 from Patent EP1572962.
JD360696 - Sequence 341720 from Patent EP1572962.
JD037497 - Sequence 18521 from Patent EP1572962.
JD204099 - Sequence 185123 from Patent EP1572962.
JD104678 - Sequence 85702 from Patent EP1572962.
JD210209 - Sequence 191233 from Patent EP1572962.
JD189540 - Sequence 170564 from Patent EP1572962.
JD133947 - Sequence 114971 from Patent EP1572962.
MP015277 - Sequence 480 from Patent WO2019016252.

-  Other Names for This Gene
  Alternate Gene Symbols: HDGL1_HUMAN, NM_138574, NP_612641, PWWP1, Q5TGJ6, Q96MJ6
UCSC ID: uc003nds.3
RefSeq Accession: NM_138574
Protein: Q5TGJ6 (aka HDGL1_HUMAN)
CCDS: CCDS34347.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_138574.2
exon count: 1CDS single in 3' UTR: no RNA size: 1073
ORF size: 756CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1694.00frame shift in genome: no % Coverage: 100.00
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.