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Odad3tm1c(EUCOMM)Hmgu
Targeted Allele Detail
Summary
Symbol: Odad3tm1c(EUCOMM)Hmgu
Name: outer dynein arm docking complex subunit 3; targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI ID: MGI:6360701
Synonyms: Ccdc151Con
Gene: Odad3  Location: Chr9:21901167-21913930 bp, - strand  Genetic Position: Chr9, 8.01 cM, cytoband A4
Alliance: Odad3tm1c(EUCOMM)Hmgu page
IMPC: Odad3 gene page
Mutation
origin
Mutant Cell Line:  HEPD0634_2_D03
Germline Transmission:  Earliest citation of germline transmission: J:278798
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Project Collection: EUCOMM
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion     Vector: L1L2_Bact_P
 
Mutation detailsThe L1L2_Bact_P cassette was inserted at position 21908891 of Chromosome 9 upstream of the critical exons 2 and 3 (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon(s) at position 21909920. The critical exons 2 and 3 thus flanked by loxP sites. A "conditional ready" (floxed) allele was created by flp recombinase expression in mice carrying this allele. Subsequent cre expression results in a knockout mouse. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml (J:278798)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Odad3 Mutation:  27 strains or lines available
References
Original:  J:278798 Chiani F, et al., Functional loss of Ccdc1 51 leads to hydrocephalus in a mouse model of primary ciliary dyskinesia. Dis Model Mech. 2019 Aug 2;12(8):dmm038489
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