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Pthlhtm1Fbe
Targeted Allele Detail
Summary
Symbol: Pthlhtm1Fbe
Name: parathyroid hormone-like peptide; targeted mutation 1, F Beck
MGI ID: MGI:2388593
Synonyms: PTHrP -
Gene: Pthlh  Location: Chr6:147153607-147165511 bp, - strand  Genetic Position: Chr6, 78.19 cM, cytoband F-G
Alliance: Pthlhtm1Fbe page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:79622
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Exon 4 was replaced with a neomycin selection cassette. (J:79622, J:112521)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 16 anatomical structure(s)
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 Pthlh Mutation:  19 strains or lines available
References
Original:  J:79622 Tucci J, et al., The role of fetal parathyroid hormone-related protein in transplacental calcium transport. J Mol Endocrinol. 1996 Oct;17(2):159-64
All:  7 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
04/09/2024
MGI 6.23
The Jackson Laboratory