Wdr47tm1b(EUCOMM)Wtsi
Targeted Allele Detail
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| Symbol: |
Wdr47tm1b(EUCOMM)Wtsi |
| Name: |
WD repeat domain 47; targeted mutation 1b, Wellcome Trust Sanger Institute |
| MGI ID: |
MGI:6102912 |
| Gene: |
Wdr47 Location: Chr3:108498595-108553035 bp, + strand Genetic Position: Chr3, 47.38 cM
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| Alliance: |
Wdr47tm1b(EUCOMM)Wtsi page
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| IMPC: |
Wdr47 gene page |
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| Mutant Cell Line: |
EPD0046_1_C04 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:249035
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| Parent Cell Line: |
JM8.F6 (ES Cell)
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| Strain of Origin: |
C57BL/6N
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| Project Collection: |
EUCOMM
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| Allele Type: |
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Targeted (Null/knockout, Reporter) |
| Mutations: |
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Insertion, Intragenic deletion
Vector: L1L2_gt0
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Mutation details: The L1L2_gt0 cassette was inserted at position 108525343 of Chromosome 3 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of the targeted exon(s) at position 108526974. The critical exon(s) is/are thus flanked by loxP sites. A null/knockout allele was created by cre recombinase expression in mice carrying the tm1a allele to remove the neo selection cassette and loxP-flanked critical exon(s).
(J:249035)
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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 Wdr47 Mutation: |
52 strains or lines available
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| Original: |
J:249035 Kannan M, et al., WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy. Proc Natl Acad Sci U S A. 2017 Oct 31;114(44):E9308-E9317 |
| All: |
2 reference(s) |
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