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Protein Coding Gene : Ide insulin degrading enzyme

Primary Identifier  MGI:96412 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  15925
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables endopeptidase activity. Involved in insulin catabolic process and insulin receptor recycling. Acts upstream of or within amyloid-beta clearance and response to oxidative stress. Located in extracellular exosome. Is active in endosome lumen. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; respiratory system; and sensory organ. Human ortholog(s) of this gene implicated in Alzheimer's disease and type 2 diabetes mellitus. Orthologous to human IDE (insulin degrading enzyme).
PHENOTYPE: Mice homozygous for a null allele show beta amyloid accumulations in the brain, hyperinsulinemia, and glucose intolerance. Mice homozygous for a different null allele show decreased testis weight, small seminiferous tubules, abnormal sperm morphology, and decreased sperm viability. [provided by MGI curators]
  • synonyms:
  • MGI:2147459,
  • Ide,
  • RIKEN cDNA 4833415K22 gene,
  • RIKEN cDNA 1300012G03 gene,
  • MGI:1914150,
  • expressed sequence AI507533,
  • MGD-MRK-11179,
  • 1300012G03Rik,
  • AI507533,
  • MGI:2147575,
  • AA675336,
  • expressed sequence AA675336,
  • 4833415K22Rik,
  • MGI:1921015,
  • insulin degrading enzyme

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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Canonical gene --> Transcripts in specific strains.

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Proteins

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Mouse features --> Functions (GO terms)

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Disease

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