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Amotl1em3Rstot
Endonuclease-mediated Allele Detail
Summary
Symbol: Amotl1em3Rstot
Name: angiomotin-like 1; endonuclease-mediated mutation 3, Rolf Stottmann
MGI ID: MGI:6276197
Synonyms: AmotlD8
Gene: Amotl1  Location: Chr9:14453262-14556352 bp, - strand  Genetic Position: Chr9, 4.12 cM, cytoband A3
Alliance: Amotl1em3Rstot page
Mutation
origin
Strain of Origin:  C57BL/6N
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsAn eight base pair deletion was introduced by CRIPSR mutagenesis. A reading frameshift results in a protein with 34 aberrant amino acids followed by a premature stop codon. (J:270029)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
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
Carrying any Amotl1 Mutation:  56 strains or lines available
References
Original:  J:270029 Liegel RP, et al., Using human sequencing to guide craniofacial research. Genesis. 2019 Jan;57(1):e23259
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory