Vgll4tm1c(EUCOMM)Hmgu
Targeted Allele Detail
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| Symbol: |
Vgll4tm1c(EUCOMM)Hmgu |
| Name: |
vestigial like family member 4; targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH |
| MGI ID: |
MGI:6360734 |
| Synonyms: |
Vgll4fl |
| Gene: |
Vgll4 Location: Chr6:114837589-114946955 bp, - strand Genetic Position: Chr6, 53.07 cM
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| Alliance: |
Vgll4tm1c(EUCOMM)Hmgu page
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| IMPC: |
Vgll4 gene page |
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| Mutant Cell Line: |
HEPD0680_7_D07 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:273437
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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: |
EUCOMM
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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 114867338 of Chromosome 6 upstream of the critical exon 2 (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 a 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 the targeted exon 2 at position 114868256. The critical exon 2 is thus flanked by loxP sites. A "conditional ready" (floxed) allele was created by flp recombinase expression in mice carrying this allele. Subsequent cre expression results in a knockout mouse. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml
(J:273437)
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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 Vgll4 Mutation: |
24 strains or lines available
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| Original: |
J:273437 Yu W, et al., VGLL4 plays a critical role in heart valve development and homeostasis. PLoS Genet. 2019 Feb;15(2):e1007977 |
| All: |
4 reference(s) |
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