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Fam20ctm1Lex
Targeted Allele Detail
Nomenclature
Symbol: Fam20ctm1Lex
Name: family with sequence similarity 20, member C; targeted mutation 1, Lexicon Genetics
MGI ID: MGI:5432377
Gene: Fam20c  Location: Chr5:138754514-138810077 bp, + strand  Genetic Position: Chr5, 77.19 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:186384
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S5/SvEvBrd
Project Collection: Lexicon
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Exon 1 including the start codon and exon 2 were replaced by a lacZ/floxed neo cassette. (J:186384)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Fam20c Mutation:  14 strains or lines available
References
Original:  J:186384 Vogel P, et al., Amelogenesis Imperfecta and Other Biomineralization Defects in Fam20a and Fam20c Null Mice. Vet Pathol. 2012 Jun 25;
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/12/2017
MGI 6.10
The Jackson Laboratory