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| Nomenclature |
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Symbol:
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Pthlhtm1Fbe
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Name:
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parathyroid hormone-like peptide;
targeted mutation 1, F Beck
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MGI ID: |
MGI:2388593 |
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Synonyms: |
PTHrP - |
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Gene:
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Pthlh
Location:
Chr6:147252101-147264167 bp, - strand
Genetic Position: Chr6,
78.19 cM, cytoband F-G
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:79622
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Parent Cell Line:
| R1 (ES Cell) |
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Strain of Origin:
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(129X1/SvJ x 129S1/Sv)F1-Kitl+
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Exon 4 was replaced with a neomycin selection cassette. (J:79622, J:112521)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Pthlh Mutation:
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1 strain or line available |
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| References |
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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
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All: |
7 reference(s)
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Analysis Tools
