Tlcd4tm1a(EUCOMM)Hmgu
Targeted Allele Detail
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| Symbol: |
Tlcd4tm1a(EUCOMM)Hmgu |
| Name: |
TLC domain containing 4; targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH |
| MGI ID: |
MGI:4435938 |
| Synonyms: |
TMEM56- |
| Gene: |
Tlcd4 Location: Chr3:120995657-121076756 bp, - strand Genetic Position: Chr3, 52.94 cM, cytoband G3
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| Alliance: |
Tlcd4tm1a(EUCOMM)Hmgu page
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| IMPC: |
Tlcd4 gene page |
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| Mutant Cell Lines: |
HEPD0529_2_B02, HEPD0529_2_B04, HEPD0529_2_C02, HEPD0529_2_C03, HEPD0529_2_E02, HEPD0529_2_E04, HEPD0529_2_G03 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:385397
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| Parent Cell Line: |
JM8.N4 (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 (Conditional ready, Null/knockout, Reporter) |
| Mutation: |
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Insertion
Vector: L1L2_Pgk_P
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Mutation details: The L1L2_Pgk_P cassette was inserted at position 121021659 of Chromosome 3 upstream of the critical exons 5 and 6 (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 PGK promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of exon 6 at position 121023041. Exons 5 and 6 are thus flanked by loxP sites. A "conditional ready" (floxed) allele can be created by flp recombinase expression in mice carrying this allele. Subsequent cre expression results in a knockout mouse. If cre expression occurs without flp expression, a reporter knockout mouse will be created. 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. qRT-PCR analysis using primer pairs covering exons 7 and 8 revealed residual expression of approximately 20-25% of wild-type levels in liver samples from adult homozygous mutant mice. Western blot analysis using an antibody specific for the C-terminal region confirmed the absence of full-length protein in homozygous mutants. No shorter protein variants corresponding to exons 7-8 were detected. This allele represents a strong hypomorphic, and likely null, mutation.
(J:157065, J:385397)
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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 Tlcd4 Mutation: |
20 strains or lines available
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| Original: |
J:157065 Helmholtz Zentrum Muenchen GmbH, Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu). MGI Direct Data Submission. 2010-2015; |
| All: |
2 reference(s) |
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