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Kif17tm1.2Wbae
Targeted Allele Detail
Summary
Symbol: Kif17tm1.2Wbae
Name: kinesin family member 17; targeted mutation 1.2, Wolfgang Baehr
MGI ID: MGI:5804008
Gene: Kif17  Location: Chr4:137989562-138029284 bp, + strand  Genetic Position: Chr4, 70.07 cM, cytoband D3
Alliance: Kif17tm1.2Wbae page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:227137
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA loxP site was inserted upstream of exon 4. An FRT-flanked neomycin resistance cassette with a 3' loxP site was inserted downstream of exon 4. Flp-mediated recombination removed the selection cassette. Cre-mediated recombination removed exon 4. Immunohistochemistry confirmed the absence of protein expression in photoreceptors. (J:227137)
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 Kif17 Mutation:  36 strains or lines available
References
Original:  J:227137 Jiang L, et al., Kinesin family 17 (osmotic avoidance abnormal-3) is dispensable for photoreceptor morphology and function. FASEB J. 2015 Dec;29(12):4866-80
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
12/30/2025
MGI 6.24
The Jackson Laboratory