nur49
Chemically induced Allele Detail

Summary

• Symbol: nur49
• Name: neurological 49
• MGI ID: MGI:3038787
• Synonyms: nur^m49Jus
• Gene: nur49 Location: unknown
• Alliance: nur49 page

Mutation origin

• Strain of Origin: Not Specified
• Project Collection: Mutagenesis for Dev. Defects

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This phenotypic mutant was identified in an ENU mutagenesis screen at the Baylor College of Medicine.
• Inheritance: Recessive

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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hm1	nur49/nur49	Not Specified

Phenotypes:

Affected Systems	hm1
show or hide all annotated terms
behavior/neurological	√
impaired limb coordination	√
abnormal gait	√

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

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
• Carrying any nur49 Mutation: 0 strains or lines available

References

• Original: J:89098 The Mouse Genome Project at The Baylor College of Medicine, Heritable mouse mutants from the Mouse Mutagenesis for Developmental Defects Program. MGI Direct Data Submission. 2004-5
• All: 1 reference(s)