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Pkhd1m1Anu
Chemically induced Allele Detail
Summary
Symbol: Pkhd1m1Anu
Name: polycystic kidney and hepatic disease 1; mutation 1, Austrailan National University
MGI ID: MGI:6357751
Synonyms: ENU8C:032
Gene: Pkhd1  Location: Chr1:20128003-20688288 bp, - strand  Genetic Position: Chr1, 6.27 cM, cytoband A2-A5
Alliance: Pkhd1m1Anu page
Mutation
origin
Strain of Origin:  C57BL/6NCrl
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsThe molecular lesion is a A to T at position 1059 on cDNA in exon 38, resulting in an Isoleucine to Phenylalanine at position 275. (J:104190)
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 Pkhd1 Mutation:  227 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
01/06/2026
MGI 6.24
The Jackson Laboratory