Kif6tm1b(KOMP)Mbp
Targeted Allele Detail
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| Symbol: |
Kif6tm1b(KOMP)Mbp |
| Name: |
kinesin family member 6; targeted mutation 1b, Mouse Biology Program, UC Davis |
| MGI ID: |
MGI:6276220 |
| Synonyms: |
Kif6-LacZtm1b |
| Gene: |
Kif6 Location: Chr17:49922164-50216875 bp, + strand Genetic Position: Chr17, 25.78 cM, cytoband C
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| Alliance: |
Kif6tm1b(KOMP)Mbp page
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| IMPC: |
Kif6 gene page |
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| Mutant Cell Line: |
EPD0736_3_G01 |
| Germline Transmission: |
Earliest citation of germline transmission:
J:269442
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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 (Null/knockout, Reporter) |
| Mutations: |
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Insertion, Intragenic deletion
Vector: L1L2_Bact_P
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Mutation details: The L1L2_Bact_P cassette was inserted at position 49977578 of Chromosome 17 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 49978471. 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). 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:269442)
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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 Kif6 Mutation: |
36 strains or lines available
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| Original: |
J:269442 Konjikusic MJ, et al., Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. PLoS Genet. 2018 Nov;14(11):e1007817 |
| All: |
1 reference(s) |
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