Tg(SOD1*G85R/EYFP)737Alho
Transgene Detail

Summary

• Symbol: Tg(SOD1*G85R/EYFP)737Alho
• Name: transgene insertion 737, Arthur L Horwich
• MGI ID: MGI:5630056
• Synonyms: G85R SOD1-YFP
• Transgene: Tg(SOD1*G85R/EYFP)737Alho Location: unknown
• Alliance: Tg(SOD1*G85R/EYFP)737Alho page

Transgene origin

• Strain of Origin: (C57BL/6J x SJL/J)F2

Transgene description

• Transgene Type: Transgenic (Humanized sequence, Inserted expressed sequence, Reporter)
• Mutation: Insertion
• Tg(SOD1*G85R/EYFP)737Alho expresses 1 gene
  Transgene expresses:
  

  Organism

  Expressed Gene

  Homolog in Mouse

  Note

  human

  SOD1 (6647)

  Sod1	(MGI:98351)

• Mutation details: A 12 kb genomic fragment of human SOD carrying the glycine to arginine substitution at amino acid 85 (G85R) fused to EYFP coding sequence through its C-terminal coding sequence in exon 5 was used as the transgene. The G85R mutation results in a misfolded protein associated with amyotrophic lateral sclerosis in humans and the mutant fusion protein behaves as a misfolded monomer. Southern blot analysis indicates that line 737 carries multiple transgene insertions. (J:144475)

Phenotypes

Key:

hm	homozygous	ht	heterozygous	tg	involves transgenes	√	phenotype observed
cn	conditional genotype	cx	complex: > 1 genome feature	ot	other: hemizygous, indeterminate,...	N	normal phenotype

Genotype/
Background:

	Allelic Composition	Genetic Background	Cell Line(s)
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tg1  Disease Model	Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho	involves: C57BL/6J * SJL/J

Phenotypes:

Affected Systems	tg1
show or hide all annotated terms
behavior/neurological	√
paralysis	√
cellular	√
abnormal autophagy	√
homeostasis/metabolism	√
abnormal autophagy	√
nervous system	√
abnormal motor neuron morphology	√
abnormal spinal cord ventral horn morphology	√
abnormal nervous system physiology	√

View phenotypes and curated references for all genotypes (concatenated display).

Disease models

Key:

√

disease model

expected model not found

Models:

Human Diseases	tg1
amyotrophic lateral sclerosis type 1 IDs amyotrophic lateral sclerosis type 1       DOID:0060193 ICD10CM:G12.2 OMIM:105400 Close	√

Expression

In Structures Affected by this Mutation:

4 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available

References

• Original: J:144475 Wang J, et al., Progressive aggregation despite chaperone associations of a mutant SOD1-YFP in transgenic mice that develop ALS. Proc Natl Acad Sci U S A. 2009 Feb 3;106(5):1392-7
• All: 7 reference(s)