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Lhfpl1tm1.1(NCOM)Mfgc
Targeted Allele Detail
Summary
Symbol: Lhfpl1tm1.1(NCOM)Mfgc
Name: lipoma HMGIC fusion partner-like 1; targeted mutation 1.1, Mammalian Functional Genomics Centre
MGI ID: MGI:5766133
Gene: Lhfpl1  Location: ChrX:144073355-144132085 bp, - strand  Genetic Position: ChrX, 66.54 cM
Alliance: Lhfpl1tm1.1(NCOM)Mfgc page
IMPC: Lhfpl1 gene page
Mutation
origin
Mutant Cell Line:  N02005P1_C_183W_F10
Germline Transmission:  Earliest citation of germline transmission: J:165964
Parent Cell Line:  C2 (Tcp) (ES Cell)
Strain of Origin:  C57BL/6N
Project Collection: NorCOMM
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion     Vector: L1L2_GOHANU
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Lhfpl1 Mutation:  4 strains or lines available
References
Original:  J:165964 Mammalian Functional Genomics Centre, Alleles produced for the NorCOMM project by the Mammalian Functional Genomics Centre (Mfgc), University of Manitoba. MGI Direct Data Submission. 2010;
All:  3 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
10/29/2024
MGI 6.24
The Jackson Laboratory