Details for: Lfng
Associated with
Other Information
Genular Protein ID: 4054406228
Symbol: LFNG_MOUSE
Name: O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9187150
Title: A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway.
PubMed ID: 9187150
PubMed ID: 9207795
Title: Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila.
PubMed ID: 9207795
DOI: 10.1038/ng0797-283
PubMed ID: 12110169
Title: Clock regulatory elements control cyclic expression of Lunatic fringe during somitogenesis.
PubMed ID: 12110169
PubMed ID: 16141072
Title: The transcriptional landscape of the mammalian genome.
PubMed ID: 16141072
PubMed ID: 10330372
Title: Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse.
PubMed ID: 10330372
PubMed ID: 10935626
Title: Fringe is a glycosyltransferase that modifies Notch.
PubMed ID: 10935626
DOI: 10.1038/35019000
PubMed ID: 12167404
Title: Lunatic fringe, FGF, and BMP regulate the Notch pathway during epithelial morphogenesis of teeth.
PubMed ID: 12167404
PubMed ID: 9690473
Title: Lunatic fringe is an essential mediator of somite segmentation and patterning.
PubMed ID: 9690473
DOI: 10.1038/28632
PubMed ID: 10341080
Title: Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes.
PubMed ID: 10341080
PubMed ID: 11520458
Title: Subversion of the T/B lineage decision in the thymus by lunatic fringe-mediated inhibition of Notch-1.
PubMed ID: 11520458
PubMed ID: 12110168
Title: Periodic Lunatic fringe expression is controlled during segmentation by a cyclic transcriptional enhancer responsive to notch signaling.
PubMed ID: 12110168
PubMed ID: 16221665
Title: Lunatic fringe, manic fringe, and radical fringe recognize similar specificity determinants in O-fucosylated epidermal growth factor-like repeats.
PubMed ID: 16221665
PubMed ID: 16385447
Title: Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.
PubMed ID: 16385447
DOI: 10.1086/498879
PubMed ID: 28089369
Title: Deciphering the fringe-mediated notch code: identification of activating and inhibiting sites allowing discrimination between ligands.
PubMed ID: 28089369
Sequence Information:
- Length: 378
- Mass: 41952
- Checksum: FD0A02597BF9AFED
- Sequence:
MLQRCGRRLL LALVGALLAC LLVLTADPPP TPMPAERGRR ALRSLAGSSG GAPASGSRAA VDPGVLTREV HSLSEYFSLL TRARRDADPP PGVASRQGDG HPRPPAEVLS PRDVFIAVKT TRKFHRARLD LLFETWISRH KEMTFIFTDG EDEALAKLTG NVVLTNCSSA HSRQALSCKM AVEYDRFIES GKKWFCHVDD DNYVNLRALL RLLASYPHTQ DVYIGKPSLD RPIQATERIS EHKVRPVHFW FATGGAGFCI SRGLALKMGP WASGGHFMST AERIRLPDDC TIGYIVEALL GVPLIRSGLF HSHLENLQQV PTTELHEQVT LSYGMFENKR NAVHIKGPFS VEADPSRFRS VHCHLYPDTP WCPRSAIF
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.