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Zfp830tm2Cota
Targeted Allele Detail
Summary
Symbol: Zfp830tm2Cota
Name: zinc finger protein 830; targeted mutation 2, Michel Cohen-Tannoudji
MGI ID: MGI:4950669
Synonyms: Omcg1trilox
Gene: Zfp830  Location: Chr11:82655171-82656761 bp, + strand  Genetic Position: Chr11, 50.22 cM
Alliance: Zfp830tm2Cota page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:171647
Parent Cell Line:  CK35 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutations:    Insertion, Single point mutation
 
Mutation detailsA loxP site was inserted upstream of the single coding exon. A floxed neo cassette was inserted downstream of the coding exon. This allele also contains a G to T transition at nucleotide 299 (GenBank accession HM446523) that results in the non-synonymous variation of valine for glycine at position 92 (G92V). (J:171647)
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 Zfp830 Mutation:  14 strains or lines available
References
Original:  J:171647 Houlard M, et al., DNA-RNA hybrids contribute to the replication dependent genomic instability induced by Omcg1 deficiency. Cell Cycle. 2011 Jan 1;10(1):108-17
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
11/12/2024
MGI 6.24
The Jackson Laboratory