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Protein Coding Gene : Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase

Primary Identifier  MGI:1095404 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  17305
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase activity. Involved in marginal zone B cell differentiation and regulation of Notch signaling pathway. Acts upstream of or within blastocyst formation and positive regulation of Notch signaling pathway. Predicted to be located in Golgi membrane. Is expressed in several structures, including alimentary system; genitourinary system; limb; nervous system; and sensory organ. Orthologous to human MFNG (MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase).
PHENOTYPE: Mice homozygous for a null mutation exhibit normal pancreatic development, morphology and physiology. Mice homozygous for a different knock-out allele exhibit altered lymphocyte numbers, abnormal circulating factors II, VII, IX and XI, and decreased prothrombin and partial thromboplastin time. [provided by MGI curators]
  • synonyms:
  • AW546563,
  • Mfng,
  • MGI:2146229,
  • MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase,
  • manic fringe,
  • expressed sequence AW546563

Features --> Cross References

Genome

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3 Involved In Mutations

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

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Gene --> Proteins

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Mouse features --> Functions (GO terms)

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Disease

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