Human Gene NLRX1 (uc001pvw.3)
  Description: Homo sapiens NLR family member X1 (NLRX1), transcript variant 1, mRNA.
RefSeq Summary (NM_024618): The protein encoded by this gene is a member of the NLR family and localizes to the outer mitochondrial membrane. The encoded protein is a regulator of mitochondrial antivirus responses. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2013].
Transcript (Including UTRs)
   Position: hg19 chr11:119,039,440-119,054,725 Size: 15,286 Total Exon Count: 10 Strand: +
Coding Region
   Position: hg19 chr11:119,042,113-119,054,148 Size: 12,036 Coding Exon Count: 9 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr11:119,039,440-119,054,725)mRNA (may differ from genome)Protein (975 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
H-INVHGNCHPRDLynxMGIneXtProt
OMIMPubMedReactomeTreefamUniProtKBWikipedia
BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: NLRX1_HUMAN
DESCRIPTION: RecName: Full=NLR family member X1; AltName: Full=Caterpiller protein 11.3; Short=CLR11.3; AltName: Full=Nucleotide-binding oligomerization domain protein 26; AltName: Full=Nucleotide-binding oligomerization domain protein 5; AltName: Full=Nucleotide-binding oligomerization domain protein 9; Flags: Precursor;
FUNCTION: Participates in antiviral signaling. Acts as a negative regulator of MAVS-mediated antiviral responses, through the inhibition of the virus-induced RLH (RIG-like helicase)-MAVS interaction (PubMed:18200010). Has no inhibitory function on NF- Kappa-B and type 1 interferon signaling pathways, but enhances NF- Kappa-B and JUN N-terminal kinase dependent signaling through the production of reactive oxygen species (PubMed:18219313).
SUBUNIT: Interacts with MAVS.
INTERACTION: Q6PDS3:Sarm1 (xeno); NbExp=2; IntAct=EBI-3893071, EBI-6117196;
SUBCELLULAR LOCATION: Mitochondrion outer membrane.
TISSUE SPECIFICITY: Ubiquitously expressed. Strongest expression in mammary gland, heart and muscle. Detected in HeLa, HEK293T, THP-1, HL-60, Raji and Jurkat cell lines (at protein level).
SIMILARITY: Belongs to the NLRP family.
SIMILARITY: Contains 7 LRR (leucine-rich) repeats.
SIMILARITY: Contains 1 NACHT domain.
SEQUENCE CAUTION: Sequence=BAB15075.1; Type=Erroneous initiation; Sequence=BAG51714.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=BAG51714.1; Type=Erroneous termination; Positions=951; Note=Translated as Trp;

-  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): NLRX1
CDC HuGE Published Literature: NLRX1

-  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: 21.35 RPKM in Esophagus - Mucosa
Total median expression: 268.60 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 -129.80239-0.543 Picture PostScript Text
3' UTR -201.60577-0.349 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
IPR007111 - NACHT_NTPase

Pfam Domains:
PF05729 - NACHT domain
PF13516 - Leucine Rich repeat

SCOP Domains:
52047 - RNI-like
52058 - L domain-like

Protein Data Bank (PDB) 3-D Structure
MuPIT help
3UN9 - X-ray MuPIT


ModBase Predicted Comparative 3D Structure on Q86UT6
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 orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000166 nucleotide binding
GO:0005515 protein binding
GO:0005524 ATP binding

Biological Process:
GO:0002376 immune system process
GO:0016032 viral process
GO:0032480 negative regulation of type I interferon production
GO:0032688 negative regulation of interferon-beta production
GO:0032715 negative regulation of interleukin-6 production
GO:0039536 negative regulation of RIG-I signaling pathway
GO:0043124 negative regulation of I-kappaB kinase/NF-kappaB signaling
GO:0045087 innate immune response
GO:0045824 negative regulation of innate immune response
GO:0050728 negative regulation of inflammatory response

Cellular Component:
GO:0005739 mitochondrion
GO:0005741 mitochondrial outer membrane
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0030054 cell junction


-  Descriptions from all associated GenBank mRNAs
  AK095247 - Homo sapiens cDNA FLJ37928 fis, clone CTONG2002709, highly similar to Homo sapiens NOD9 protein (NOD9), transcript variant 1, mRNA.
BX647705 - Homo sapiens mRNA; cDNA DKFZp686K08201 (from clone DKFZp686K08201).
AB094095 - Homo sapiens DLNB26 mRNA, complete cds.
BC023974 - Homo sapiens cDNA clone IMAGE:3925842, containing frame-shift errors.
AK303002 - Homo sapiens cDNA FLJ61648 complete cds, highly similar to Homo sapiens NOD9 protein (NOD9), transcript variant 2, mRNA.
AK291716 - Homo sapiens cDNA FLJ78673 complete cds, highly similar to Homo sapiens NOD9 protein (NOD9), transcript variant 1, mRNA.
BC110890 - Homo sapiens NLR family member X1, mRNA (cDNA clone MGC:131937 IMAGE:4937963), complete cds.
JD123875 - Sequence 104899 from Patent EP1572962.
JD341693 - Sequence 322717 from Patent EP1572962.
AY245437 - Homo sapiens NOD26 (NOD26) mRNA, complete cds.
EF452237 - Homo sapiens NOD5 mRNA, complete cds.
AK056454 - Homo sapiens cDNA FLJ31892 fis, clone NT2RP7003629, highly similar to Homo sapiens NOD9 protein (NOD9), transcript variant 1, mRNA.
BC013199 - Homo sapiens NLR family member X1, mRNA (cDNA clone IMAGE:4387619), partial cds.
CU680548 - Synthetic construct Homo sapiens gateway clone IMAGE:100017459 5' read NLRX1 mRNA.
KJ903195 - Synthetic construct Homo sapiens clone ccsbBroadEn_12589 NLRX1 gene, encodes complete protein.
AK025131 - Homo sapiens cDNA: FLJ21478 fis, clone COL05012.
AK225223 - Homo sapiens mRNA for NOD9 protein isoform 1 variant, clone: COL05012.
JD318921 - Sequence 299945 from Patent EP1572962.
JD398952 - Sequence 379976 from Patent EP1572962.
JD159989 - Sequence 141013 from Patent EP1572962.
JD358131 - Sequence 339155 from Patent EP1572962.
JD488345 - Sequence 469369 from Patent EP1572962.
JD112988 - Sequence 94012 from Patent EP1572962.
AL049456 - Homo sapiens mRNA; cDNA DKFZp586D2422 (from clone DKFZp586D2422).
JD560145 - Sequence 541169 from Patent EP1572962.
JD525270 - Sequence 506294 from Patent EP1572962.
JD149955 - Sequence 130979 from Patent EP1572962.
JD379465 - Sequence 360489 from Patent EP1572962.
JD449788 - Sequence 430812 from Patent EP1572962.
JD275914 - Sequence 256938 from Patent EP1572962.
JD403130 - Sequence 384154 from Patent EP1572962.
JD513171 - Sequence 494195 from Patent EP1572962.
JD539367 - Sequence 520391 from Patent EP1572962.
JD092832 - Sequence 73856 from Patent EP1572962.
JD449883 - Sequence 430907 from Patent EP1572962.
JD399181 - Sequence 380205 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa04622 - RIG-I-like receptor signaling pathway

Reactome (by CSHL, EBI, and GO)

Protein Q86UT6 (Reactome details) participates in the following event(s):

R-HSA-936564 NLRX1 inhibits MAVS-DDX58 interaction.
R-HSA-936440 Negative regulators of DDX58/IFIH1 signaling
R-HSA-168928 DDX58/IFIH1-mediated induction of interferon-alpha/beta
R-HSA-168249 Innate Immune System
R-HSA-168256 Immune System

-  Other Names for This Gene
  Alternate Gene Symbols: A8K6Q1, B3KPK2, B3KTA2, NLRX1_HUMAN, NM_024618, NOD26, NOD5, NOD9, NP_078894, Q7RTR3, Q86UT6, Q96D51, Q9H724
UCSC ID: uc001pvw.3
RefSeq Accession: NM_024618
Protein: Q86UT6 (aka NLRX1_HUMAN)
CCDS: CCDS8416.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_024618.2
exon count: 10CDS single in 3' UTR: no RNA size: 3761
ORF size: 2928CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 5815.00frame shift in genome: no % Coverage: 99.55
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.