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Heritable Phenotypic Marker : Wld wallerian degeneration
Primary Identifier  MGI:98952 Organism  mouse, laboratory
Chromosome  4 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Wallerian degeneration is important in axon regeneration initiation. C57BL/Ola mice carry a mutation for slow Wallerian degeneration resulting in slower regeneration of sciatic sensory axons when they are cut or crushed. Age affects expression and older C57BL/Ola show faster Wallerian degeneration. [provided by MGI curators]
  • synonyms:
  • Wld,
  • Wlds,
  • MGD-MRK-15436,
  • wallerian degeneration
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

13 Transgenic Expressors

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.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For





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