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Xrcc6avon
Chemically induced Allele Detail
Summary
Symbol: Xrcc6avon
Name: X-ray repair complementing defective repair in Chinese hamster cells 6; avon
MGI ID: MGI:4458398
Synonyms: ENU11B6:178a
Gene: Xrcc6  Location: Chr15:81872036-81924286 bp, + strand  Genetic Position: Chr15, 38.33 cM, cytoband E-F
Alliance: Xrcc6avon page
Mutation
origin
Strain of Origin:  C57BL/6JAnu
Project Collection: APF ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThe mutation comprises a T to C transition at nucleotide position 1494 of the mRNA sequence that results in replacement of leucine by proline at amino acid position 467 of the protein (L467P). (J:104190)
Inheritance:    Recessive
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 Xrcc6 Mutation:  63 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
10/29/2024
MGI 6.24
The Jackson Laboratory