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Spag17pcdo
Chemically induced Allele Detail
Summary
Symbol: Spag17pcdo
Name: sperm associated antigen 17; primary ciliary dyskinesia only
MGI ID: MGI:6478923
Synonyms: Spag17c.5236A>T
Gene: Spag17  Location: Chr3:99792722-100050638 bp, + strand  Genetic Position: Chr3, 43.25 cM, cytoband F3
Alliance: Spag17pcdo page
Mutation
origin
Strain of Origin:  Not Applicable
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsThis ENU-induced mutation is a c.5236A>T substitution that creates a nonsense mutation at lysine codon 1746 (p.K1746*). (J:297491)
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 Spag17 Mutation:  107 strains or lines available
References
Original:  J:297491 Abdelhamed Z, et al., A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Dis Model Mech. 2020 Oct 30;13(10):dmm045344
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
01/28/2026
MGI 6.24
The Jackson Laboratory