Human Gene C1orf131 (uc001hul.3)
  Description: Homo sapiens chromosome 1 open reading frame 131 (C1orf131), mRNA.
Transcript (Including UTRs)
   Position: hg19 chr1:231,359,509-231,376,924 Size: 17,416 Total Exon Count: 7 Strand: -
Coding Region
   Position: hg19 chr1:231,360,025-231,376,887 Size: 16,863 Coding Exon Count: 7 

Page IndexSequence and LinksPrimersGenetic AssociationsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesmRNA Descriptions
Other NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:231,359,509-231,376,924)mRNA (may differ from genome)Protein (293 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCHPRDLynxMGI
PubMedTreefamUniProtKBBioGrid 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): C1orf131
CDC HuGE Published Literature: C1orf131
Positive Disease Associations: Cholesterol, LDL , Insulin Resistance
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. Insulin Resistance
    James B Meigs et al. BMC medical genetics 2007, Genome-wide association with diabetes-related traits in the Framingham Heart Study., BMC medical genetics. [PubMed 17903298]
    Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.

-  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: 4.30 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 115.01 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 -17.2037-0.465 Picture PostScript Text
3' UTR -125.59516-0.243 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:
PF15375 - Domain of unknown function (DUF4602)

ModBase Predicted Comparative 3D Structure on Q8NDD1-2
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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
  KJ903741 - Synthetic construct Homo sapiens clone ccsbBroadEn_13135 C1orf131 gene, encodes complete protein.
BC053609 - Homo sapiens chromosome 1 open reading frame 131, mRNA (cDNA clone IMAGE:6015250), partial cds.
BC036800 - Homo sapiens chromosome 1 open reading frame 131, mRNA (cDNA clone MGC:46269 IMAGE:5589128), complete cds.
BC062353 - Homo sapiens chromosome 1 open reading frame 131, mRNA (cDNA clone MGC:71140 IMAGE:4648754), complete cds.
AL834274 - Homo sapiens mRNA; cDNA DKFZp547B1713 (from clone DKFZp547B1713).
AY358235 - Homo sapiens clone DNA142988 LTLL9335 (UNQ9335) mRNA, complete cds.
JD510213 - Sequence 491237 from Patent EP1572962.
JD549651 - Sequence 530675 from Patent EP1572962.
JD289725 - Sequence 270749 from Patent EP1572962.
JD405012 - Sequence 386036 from Patent EP1572962.
JD352137 - Sequence 333161 from Patent EP1572962.
JD346980 - Sequence 328004 from Patent EP1572962.
CU691424 - Synthetic construct Homo sapiens gateway clone IMAGE:100016645 5' read C1orf131 mRNA.
JD065424 - Sequence 46448 from Patent EP1572962.
AK303359 - Homo sapiens cDNA FLJ61512 complete cds.
AK055124 - Homo sapiens cDNA FLJ30562 fis, clone BRAWH2004731.
JD020485 - Sequence 1509 from Patent EP1572962.
JD035167 - Sequence 16191 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: NM_152379, NP_689592, Q8NDD1-2
UCSC ID: uc001hul.3
RefSeq Accession: NM_152379
Protein: Q8NDD1-2, splice isoform of Q8NDD1 CCDS: CCDS1591.2

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_152379.2
exon count: 7CDS single in 3' UTR: no RNA size: 1486
ORF size: 882CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1961.00frame shift in genome: no % Coverage: 96.57
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.