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Drd2m1Anu
Chemically induced Allele Detail
Summary
Symbol: Drd2m1Anu
Name: dopamine receptor D2; mutation 1, Australian National University
MGI ID: MGI:5570458
Synonyms: ENU23:037:DRD2
Gene: Drd2  Location: Chr9:49251927-49319477 bp, + strand  Genetic Position: Chr9, 26.72 cM
Alliance: Drd2m1Anu page
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 237 of the cDNA sequence (transcript Drd2-201; ENSMUST00000075764), resulting in replacement of isoleucine by threonine at amino acid position 48 of the protein (I48T). (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: 1 strain available      Cell Lines: 0 lines available
Carrying any Drd2 Mutation:  70 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
04/16/2024
MGI 6.23
The Jackson Laboratory