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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tph1tm1Kry
targeted mutation 1, Gerard Karsenty
MGI:3837399
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Lrp5tm1Kry/Lrp5tm1Kry
Tph1tm1Kry/Tph1+
Tg(Vil1-cre)20Syr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 MGI:3837415
cn2
Htr1btm1Rhn/Htr1b+
Tph1tm1Kry/Tph1+
Tg(Vil1-cre)20Syr/0
involves: 129S2/SvPas * C57BL/6 * DBA/2 MGI:3837413
cn3
Tph1tm1Kry/Tph1tm1Kry
Tg(Vil1-cre)20Syr/0
involves: C57BL/6 * DBA/2 MGI:3837407
cn4
Tph1tm1Kry/Tph1tm1Kry
Tg(Col1a1-cre)1Kry/0
involves: FVB MGI:3837408


Genotype
MGI:3837415
cn1
Allelic
Composition
Lrp5tm1Kry/Lrp5tm1Kry
Tph1tm1Kry/Tph1+
Tg(Vil1-cre)20Syr/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp5tm1Kry mutation (0 available); any Lrp5 mutation (81 available)
Tg(Vil1-cre)20Syr mutation (3 available)
Tph1tm1Kry mutation (0 available); any Tph1 mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
N
• loss of expression of 1 copy of Tph1 in the gut rescues the bone phenotype seen in Lrp5 null mice




Genotype
MGI:3837413
cn2
Allelic
Composition
Htr1btm1Rhn/Htr1b+
Tph1tm1Kry/Tph1+
Tg(Vil1-cre)20Syr/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr1btm1Rhn mutation (3 available); any Htr1b mutation (27 available)
Tg(Vil1-cre)20Syr mutation (3 available)
Tph1tm1Kry mutation (0 available); any Tph1 mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• phenotype is the same as in mice homozygous null for Htr1b and mice conditional null for Tph1 in the gut




Genotype
MGI:3837407
cn3
Allelic
Composition
Tph1tm1Kry/Tph1tm1Kry
Tg(Vil1-cre)20Syr/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Vil1-cre)20Syr mutation (3 available)
Tph1tm1Kry mutation (0 available); any Tph1 mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• increased osteoblast proliferation

homeostasis/metabolism
• decreased circulating serotonin levels

skeleton
• increased osteoblast proliferation
• severe
• ovariectomy does not result in decreased bone mass unlike in controls
• increased bone formation




Genotype
MGI:3837408
cn4
Allelic
Composition
Tph1tm1Kry/Tph1tm1Kry
Tg(Col1a1-cre)1Kry/0
Genetic
Background
involves: FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Col1a1-cre)1Kry mutation (2 available)
Tph1tm1Kry mutation (0 available); any Tph1 mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• unlike mice with conditional deletion in the gut, mice with conditional expression in osteoblasts have normal circulating serotonin levels

skeleton
N
• unlike mice with conditional deletion in the gut, mice with conditional expression in osteoblasts have no significant increase in bone mass or osteoblast proliferation





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory