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Symbol: |
Cryba1tm1a(EUCOMM)Hmgu |
Name: |
crystallin, beta A1; targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH |
MGI ID: |
MGI:4951042 |
Synonyms: |
beta3-, betaA3 KO |
Gene: |
Cryba1 Location: Chr11:77609441-77616109 bp, - strand Genetic Position: Chr11, 46.74 cM, cytoband B-C1
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Alliance: |
Cryba1tm1a(EUCOMM)Hmgu page
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IMPC: |
Cryba1 gene page |
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Nuclear cataracts in Cryba1tm1a(EUCOMM)Hmgu/Cryba1tm1a(EUCOMM)Hmgu mice
Show the 8 phenotype image(s) involving this allele.
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Mutant Cell Lines: |
HEPD0727_4_A03, HEPD0727_4_B04, HEPD0727_4_C03, HEPD0727_4_C04, HEPD0727_4_D04, HEPD0727_4_E01, HEPD0727_4_F03, HEPD0727_4_F04, HEPD0727_4_G02, HEPD0727_4_G03, HEPD0727_4_H01, HEPD0727_4_H02, HEPD0727_4_H03 |
Germline Transmission: |
Earliest citation of germline transmission:
J:235696
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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, Hypomorph, Null/knockout, Reporter) |
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 77611369 of Chromosome 11 upstream of the critical exon(s) (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(s) at position 77612125. The critical exon(s) is/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
(J:157065)
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Generation of the Cryba1tm1a(EUCOMM)Hmgu allele |
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View phenotypes and curated references for all genotypes (concatenated display).
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Special note about the mutation generated in J:235696: qRT-PCR analysis confirmed the absence of mRNA transcripts in homozygous mutant lenses. Western blot analysis using a polyclonal anti-betaA3-crystallin antibody revealed that reactivity corresponding to a dimer (50 kDa) is completely absent in homozygous lenses and reduced to 50% in heterozygous lenses. However, a band of severely reduced intensity is still detectable in homozygous lenses at the 25 kDa position. Similar results are observed using a monoclonal antibody, suggesting that a small amount of protein is still produced in homozygous lenses.
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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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