fmt
Gene Detail

Symbol Name ID

fmt formentin MGI:95565

Feature Type

heritable phenotypic marker

Genetic Map

Chromosome Unknown

Alleles and phenotypes

All alleles(1) : Spontaneous(1)
 

Mutations in this gene result in loss of coordination.

 

References

(Earliest) J:13971 Guenet JL, Formentin: (fmt) a new recessive neurological mutation. Mouse News Lett. 1984;70:95
All references(1)

Other accession IDs

MGD-MRK-9846