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LFNG information


Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe, also known as Lunatic Fringe, is a protein encoded in humans by the LFNG gene.[1][2][3]

LFNG
Identifiers
AliasesLFNG, SCDO3, LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
External IDsOMIM: 602576; MGI: 1095413; HomoloGene: 22475; GeneCards: LFNG; OMA:LFNG - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002304
NM_001040167
NM_001040168
NM_001166355

NM_008494

RefSeq (protein)

NP_001035257
NP_001035258
NP_001159827
NP_002295

NP_032520

Location (UCSC)Chr 7: 2.51 – 2.53 MbChr 5: 140.59 – 140.6 Mb
PubMed search[6][7]
Wikidata
View/Edit HumanView/Edit Mouse

This gene encodes a member of the glycosyltransferase superfamily. The encoded protein is a single-pass type II Golgi membrane protein that functions as a fucose-specific glycosyltransferase, adding an N-acetylglucosamine to the fucose residue of a group of signaling receptors involved in regulating cell fate decisions during development. Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. Alternatively spliced transcript variants that encode different isoforms have been described, however, not all variants have been fully characterized.[3]

  1. ^ "LFNG - Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe - Homo sapiens (Human) - LFNG gene & protein". www.uniprot.org. Retrieved 4 June 2022.
  2. ^ Egan S, Herbrick JA, Tsui LC, Cohen B, Flock G, Beatty B, Scherer SW (December 1998). "Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12". Genomics. 54 (3): 576–7. doi:10.1006/geno.1998.5559. PMID 9878264.
  3. ^ a b "Entrez Gene: LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase".
  4. ^ a b c GRCh38: Ensembl release 89: ENSG00000106003 – Ensembl, May 2017
  5. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029570 – Ensembl, May 2017
  6. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  7. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

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LFNG

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fringe, also known as Lunatic Fringe, is a protein encoded in humans by the LFNG gene. This gene encodes a member of the glycosyltransferase superfamily....

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Somite

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activation turns on LFNG which in turn inhibits the Notch receptor. Notch activation also turns on the HES1 gene which inactivates LFNG, re-enabling the...

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Lunatic fringe

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fanatical views, may refer to: "Lunatic Fringe" (song), a 1981 song by Red Rider LFNG, a gene in the Notch pathway Jon Moxley (born 1985), nicknamed "Lunatic Fringe"...

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three genes associated to the mouse segmentation clock, (MESP2, DLL3 and LFNG), have been shown to be mutated in cases of congenital scoliosis, suggesting...

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Vias LFMU BZR Béziers Cap d'Agde Airport Public Montpellier / Candillargues LFNG Montpellier - Candillargues Airport Public Montpellier / Mauguio LFMT MPL...

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Notch signaling pathway

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coordinate key steps in this process. In mice, mutations in Notch1, Dll1 or Dll3, Lfng, or Hes7 result in abnormal somite formation. Similarly, in humans, the following...

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HES7 gene

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oscillatory manner. The HES7 protein also represses expression of Lunatic Fringe (LFNG) thereby both directly and indirectly regulating the Notch signalling pathway...

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Fringe gene

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the manic fringe (MFNG), the radical fringe (RFNG) and lunatic fringe (LFNG) genes were identified in mammals. Fringe genes encode O-fucose specific...

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Spondylocostal dysostosis

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Type OMIM Gene Locus SCDO1 277300 DLL3 19q13 SCDO2 608681 MESP2 15q26.1 SCDO3 609813 LFNG 7p22 SCDO4 122600 GDF6 8q22.1...

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Kenro Kusumi

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and he contributed to subsequent research identifying mutations in the LFNG and HES7 genes for related congenital axial skeletal disorders. Kusumi is...

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MFNG

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family which also includes the radical fringe (RFNG) and lunatic fringe (LFNG). They all encode evolutionarily conserved proteins that act in the Notch...

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Zona limitans intrathalamica

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respectively. The ZLI is also characterized by a lack of lunatic fringe (lfng), which is observable even before Shh expression is observed in the forming...

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List of OMIM disorder codes

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608681; MESP2 Spondylocostal dysostosis, autosomal recessive 3; 609813; LFNG Spondylocostal dysostosis, autosomal recessive, 1; 277300; DLL3 Spondylocostal...

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