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nmf111
Chemically induced Allele Detail

Nomenclature
Symbol: nmf111
Name: neuroscience mutagenesis facility, 111
MGI ID: MGI:2678255
Gene: nmf111   Location: unknown     Genetic Position: Chr4, 30.0 cM
Mutation
origin
Strain of Origin: C57BL/6J
Mutation
description
Allele Type: Chemically induced (ENU)
Mutation: Undefined
  This phenotypic mutant was identified in an ENU mutagenesis screen. (J:82238)
Inheritance: Recessive
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any nmf111 Mutation: 2 strains or lines available
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

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Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
hm1
  
behavior/neurological          
  
growth/size          
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   
nmf111/nmf111 C57BL/6J
References
Original: J:82238 JAX Neuroscience Mutagenesis Facility URL: http://www.jax.org/nmf, "Heritable mouse mutants from JAX NMF ENU Mutagenesis Program" MGI Direct Data Submission 2003;():
All: 1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/20/2009
MGI_4.31
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