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Allele : Agrn<nmf380> agrin; neuroscience mutagenesis facility, 380

Primary Identifier  MGI:3614578 Allele Type  Chemically induced (ENU)
Gene  Agrn Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  This phenotypic mutation was identified in an ENU mutagenesis screen. The molecular mutation is an A to G conversion, resulting in the change of phenylalanine 1061 to serine (F1061S, numbered according to the SN form of the protein) in the SEA domain of the encoded protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • NMF380,
  • NMF380
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

6 Publication categories