Wdfy3tm1c(KOMP)Mbp
Targeted Allele Detail
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| Symbol: |
Wdfy3tm1c(KOMP)Mbp |
| Name: |
WD repeat and FYVE domain containing 3; targeted mutation 1c, Mouse Biology Program, UC Davis |
| MGI ID: |
MGI:5795593 |
| Synonyms: |
Wdfy3loxP |
| Gene: |
Wdfy3 Location: Chr5:101980822-102217787 bp, - strand Genetic Position: Chr5, 48.95 cM
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| Alliance: |
Wdfy3tm1c(KOMP)Mbp page
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| IMPC: |
Wdfy3 gene page |
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| Mutant Cell Line: |
DEPD00523_5_G11 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:225200
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| Parent Cell Line: |
JM8A3.N1 (ES Cell)
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| Strain of Origin: |
C57BL/6N-Atm1Brd
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| Project Collection: |
KOMP-CSD
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| Allele Type: |
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Targeted (Conditional ready, No functional change) |
| Mutation: |
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Insertion
Vector: L1L2_Bact_P
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Mutation details: The L1L2_Bact_P cassette was inserted at position 102100564 of Chromosome 5 upstream of the critical exon (exon 8) (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 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 exon 8 at position 102101479. A "conditional ready" (floxed) allele was created by flp recombinase expression in mice, resulting in the deletion of the lacZ sequence and neomycin selection cassette. Exon 8 remains flanked by loxP sites.
(J:225200)
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Generation of the Wdfy3tm1a(KOMP)Mbp and Wdfy3tm1c(KOMP)Mbp alleles |
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View phenotypes and curated references for all genotypes (concatenated display).
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| 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
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| Carrying any Wdfy3 Mutation: |
210 strains or lines available
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| Original: |
J:225200 Orosco LA, et al., Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology. Nat Commun. 2014;5:4692 |
| All: |
3 reference(s) |
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