Human Gene FMR1NB (uc004fcm.3)
  Description: Homo sapiens fragile X mental retardation 1 neighbor (FMR1NB), mRNA.
Transcript (Including UTRs)
   Position: hg19 chrX:147,062,849-147,108,187 Size: 45,339 Total Exon Count: 6 Strand: +
Coding Region
   Position: hg19 chrX:147,062,923-147,106,520 Size: 43,598 Coding Exon Count: 5 

Page IndexSequence and LinksUniProtKB CommentsPrimersCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chrX:147,062,849-147,108,187)mRNA (may differ from genome)Protein (255 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
H-INVHGNCHPRDLynxMGIneXtProt
PubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: FMR1N_HUMAN
DESCRIPTION: RecName: Full=Fragile X mental retardation 1 neighbor protein; AltName: Full=Cancer/testis antigen 37; Short=CT37; AltName: Full=Sarcoma antigen NY-SAR-35;
SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein (Potential).
TISSUE SPECIFICITY: Testis-specific. Expressed in melanoma, sarcoma, lung, breast, bladder, esophageal and ovarian cancers.
SIMILARITY: Contains 1 P-type (trefoil) 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


-  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: 52.27 RPKM in Testis
Total median expression: 52.53 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 -29.6074-0.400 Picture PostScript Text
3' UTR -36.80179-0.206 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
IPR000519 - P_trefoil

ModBase Predicted Comparative 3D Structure on Q8N0W7
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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 orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Cellular Component:
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  BC034320 - Homo sapiens fragile X mental retardation 1 neighbor, mRNA (cDNA clone MGC:42907 IMAGE:4836772), complete cds.
AY211917 - Homo sapiens sarcoma antigen NY-SAR-35 mRNA, complete cds.
AK098602 - Homo sapiens cDNA FLJ25736 fis, clone TST05681.
JD055090 - Sequence 36114 from Patent EP1572962.
HQ447121 - Synthetic construct Homo sapiens clone IMAGE:100070408; CCSB002328_01 fragile X mental retardation 1 neighbor (FMR1NB) gene, encodes complete protein.
KJ895701 - Synthetic construct Homo sapiens clone ccsbBroadEn_05095 FMR1NB gene, encodes complete protein.
JD090246 - Sequence 71270 from Patent EP1572962.
LF380539 - JP 2014500723-A/188042: Polycomb-Associated Non-Coding RNAs.
LF380551 - JP 2014500723-A/188054: Polycomb-Associated Non-Coding RNAs.
JD203260 - Sequence 184284 from Patent EP1572962.
JD172580 - Sequence 153604 from Patent EP1572962.
JD287682 - Sequence 268706 from Patent EP1572962.
JD161795 - Sequence 142819 from Patent EP1572962.
LF380552 - JP 2014500723-A/188055: Polycomb-Associated Non-Coding RNAs.
MA616116 - JP 2018138019-A/188042: Polycomb-Associated Non-Coding RNAs.
MA616128 - JP 2018138019-A/188054: Polycomb-Associated Non-Coding RNAs.
MA616129 - JP 2018138019-A/188055: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: D3DWT3, FMR1N_HUMAN, NM_152578, NP_689791, Q8N0W7
UCSC ID: uc004fcm.3
RefSeq Accession: NM_152578
Protein: Q8N0W7 (aka FMR1N_HUMAN)
CCDS: CCDS14683.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_152578.2
exon count: 6CDS single in 3' UTR: no RNA size: 1021
ORF size: 768CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1459.00frame 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.