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Lmf1cld
Spontaneous Allele Detail
Summary
Symbol: Lmf1cld
Name: lipase maturation factor 1; combined lipase deficiency
MGI ID: MGI:1856820
Synonyms: cld
Gene: Lmf1  Location: Chr17:25798059-25881800 bp, + strand  Genetic Position: Chr17, 12.7 cM, cytoband A3.3
Alliance: Lmf1cld page
Mutation
origin
Mutation
description
Allele Type:    Spontaneous
Mutation:    Viral insertion
 
Mutation detailsThis mutation was found as a "parasitic lethal" in tw73 and recovered from the haplotype by recombination. A full-length murine endogenous retrovirus (MuERV) is inserted into intron 7. This results in the expression of an aberrant mRNA that contains sequences derived from exons 1-7, but is missing sequences derived from exons 8-11. 400 bp of viral sequence replaced the missing sequences in the mRNA. (J:115044, J:130178)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Lmf1 Mutation:  30 strains or lines available
Notes
Lmf1 tw73lab is one of three spontaneous, recessive, lethal mutations found in a wild-derived t haplotype. The other mutations are tw73 and tw73lab.
References
Original:  J:7083 Paterniti JR Jr, et al., Combined lipase deficiency (cld): a lethal mutation on chromosome 17 of the mouse. Science. 1983 Jul 8;221(4606):167-9
All:  11 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
04/16/2024
MGI 6.23
The Jackson Laboratory