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Lhfpl7m1Mhda
Chemically induced Allele Detail
Summary
Symbol: Lhfpl7m1Mhda
Name: LHFPL tetraspan subfamily member 7; mutation 1, Martin Hrabe de Angelis
MGI ID: MGI:5818772
Synonyms: Tmem211L86PMhda
Gene: Lhfpl7  Location: Chr5:113374775-113387129 bp, + strand  Genetic Position: Chr5, 55.43 cM
Alliance: Lhfpl7m1Mhda page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsThe molecular lesion is a T-to-C missense mutation (257T-C) in codon 86 in exon 4. This is predicted to alter amino acid 86 from a leucine to a proline (L86P) in the encoded protein. (J:237905)
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 Lhfpl7 Mutation:  10 strains or lines available
References
Original:  J:237905 Sabrautzki S, et al., Alleles produced by the Munich ENU mutagenesis project. MGI Direct Data Submission. 2017;
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
08/27/2024
MGI 6.24
The Jackson Laboratory