Urm1em1(IMPC)J
Endonuclease-mediated Allele Detail
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| Symbol: |
Urm1em1(IMPC)J |
| Name: |
ubiquitin related modifier 1; endonuclease-mediated mutation 1, Jackson |
| MGI ID: |
MGI:6385665 |
| Synonyms: |
Urm1- |
| Gene: |
Urm1 Location: Chr2:29717401-29735008 bp, + strand Genetic Position: Chr2, 20.67 cM, cytoband B
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| Alliance: |
Urm1em1(IMPC)J page
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| IMPC: |
Urm1 gene page |
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Urm1em1(IMPC)J/Urm1em1(IMPC)J embryos are small and developmentally delayed. Almost all E9.5 embryos display incomplete turning and abnormal head shape and most have abnormal branchial arches. Half of E9.5 embryos have abnormal cranial neural tube closure, abnormal cardiac development and slight neural tube kinking. E10.5 embryos not dying have abnormal head and slight neural tube kinking.
Show the 6 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 TTTGCACTGGGCACAGTTTT and ACAATCAGAACCCCAGGACG, which resulted in a 212 bp deletion beginning at Chromosome 2 position 29,841,335 bp and ending after 29,841,546 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001234693 (exon 3) and 130 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 35 and early truncation 7 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 Urm1em1(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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