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Spata7tm2Mrd
Targeted Allele Detail
Summary
Symbol: Spata7tm2Mrd
Name: spermatogenesis associated 7; targeted mutation 2, Graeme Mardon
MGI ID: MGI:6386672
Synonyms: Spata7Flox
Gene: Spata7  Location: Chr12:98594416-98636074 bp, + strand  Genetic Position: Chr12, 49.88 cM
Alliance: Spata7tm2Mrd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:279827
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA neomycin resistance cassette with a 5' loxP site and two 3' FRT sites was inserted upstream of exon 1. An additional loxP site was inserted downstream of exon 5. (J:279827)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Spata7 Mutation:  27 strains or lines available
References
Original:  J:279827 Eblimit A, et al., Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. Exp Eye Res. 2018 Jan;166:120-130
All:  2 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