Kctd5em1(IMPC)J
Endonuclease-mediated Allele Detail
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| Symbol: |
Kctd5em1(IMPC)J |
| Name: |
potassium channel tetramerisation domain containing 5; endonuclease-mediated mutation 1, Jackson |
| MGI ID: |
MGI:6283649 |
| Synonyms: |
Kctd5- |
| Gene: |
Kctd5 Location: Chr17:24266708-24292459 bp, - strand Genetic Position: Chr17, 12.22 cM, cytoband A3.3
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| Alliance: |
Kctd5em1(IMPC)J page
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| IMPC: |
Kctd5 gene page |
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Kctd5em1(IMPC)J/Kctd5em1(IMPC)J embryos exhibit head, heart, embryo turning and posterior cranial neural tube and yolk sac vascularization defects and are developmentally delayed.
Show the 4 phenotype image(s) involving this allele.
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| Strain of Origin: |
C57BL/6NJ
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| Project Collection: |
IMPC
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| Allele Type: |
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Endonuclease-mediated (Null/knockout) |
| Mutation: |
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Intragenic deletion
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Mutation details: This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences GCATCTTCACTCTCCCCAGC and TCACTAGACATACTTACGGA, which resulted in a 583 bp deletion beginning at Chromosome 17 position 24,058,991 bp and ending after 24,059,573 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001262470 (exon 3) and 491 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 120 and early truncation 30 amino acids later.
(J:188991)
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| Inheritance: |
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Not Specified |
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Strategy for the generation of the Kctd5em1(IMPC)J allele. |
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View phenotypes and curated references for all genotypes (concatenated display).
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| Original: |
J:188991 The Jackson Laboratory, Alleles produced for the KOMP project by The Jackson Laboratory. MGI Direct Data Submission. 2012; |
| All: |
4 reference(s) |
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