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Nr4a1m1Anu
Chemically induced Allele Detail
Nomenclature
Symbol: Nr4a1m1Anu
Name: nuclear receptor subfamily 4, group A, member 1; mutation 1, The Australian National University
MGI ID: MGI:5570322
Synonyms: ANU:ENU22:Nr4a1
Gene: Nr4a1  Location: Chr15:101254269-101274795 bp, + strand  Genetic Position: Chr15, 56.64 cM, cytoband F
Mutation
origin
Strain of Origin:  C57BL/6NCrlAnu
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Applicable)
Mutation:    Single point mutation
 
Mutation detailsThis ENU induced mutation has been identified as a T-to-C transition in exon 2, at nucleotide position 943 of the cDNA sequence (transcript Nr4a-201; ENSMUST00000023779), resulting in replacement of valine by alanine at amino acid position 272 of the protein (V272A). (J:104190)
Phenotypes
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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: 2 strains available      Cell Lines: 0 lines available
Carrying any Nr4a1 Mutation:  29 strains or lines available
References
Original:  J:104190 The Australian Phenomics Facility at The Australian National University, Heritable mouse mutants from the ENU mutagenesis program at the Australian Phenomics Facility at The Australian National University. MGI Direct Data Submission. 2006-2014;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory