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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ptgdstm1Ohy
targeted mutation 1, Osamu Hayaishi
MGI:2657199
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ptgdstm1Ohy/Ptgdstm1Ohy B6.129P2-Ptgdstm1Ohy MGI:5517580
hm2
Ptgdstm1Ohy/Ptgdstm1Ohy involves: 129P2/OlaHsd * C57BL/6 MGI:2657201
cx3
ApcMin/Apc+
Ptgdstm1Ohy/Ptgdstm1Ohy
involves: 129P2/OlaHsd * C57BL/6J MGI:3700062


Genotype
MGI:5517580
hm1
Allelic
Composition
Ptgdstm1Ohy/Ptgdstm1Ohy
Genetic
Background
B6.129P2-Ptgdstm1Ohy
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptgdstm1Ohy mutation (0 available); any Ptgds mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• transferred bone marrow mast cells are able to restore passive cutaneous anaphylaxis response in KitW-sh homozygotes
• fewer degranulating ear mast cells in a model of IgE antigen-dependent passive cutaneous anaphylaxis despite normal numbers of mast cells
• immature with less histamine
• in dermal mast cells
• in a model of IgE antigen-dependent passive cutaneous anaphylaxis, mice exhibit decreased dye extravasation (a measure of edema) compared with wild-type mice

integument
• immature with less histamine

homeostasis/metabolism
• in a model of IgE antigen-dependent passive cutaneous anaphylaxis, mice exhibit decreased dye extravasation (a measure of edema) compared with wild-type mice

hematopoietic system
• fewer degranulating ear mast cells in a model of IgE antigen-dependent passive cutaneous anaphylaxis despite normal numbers of mast cells
• immature with less histamine
• in dermal mast cells

cellular
• fewer degranulating ear mast cells in a model of IgE antigen-dependent passive cutaneous anaphylaxis despite normal numbers of mast cells




Genotype
MGI:2657201
hm2
Allelic
Composition
Ptgdstm1Ohy/Ptgdstm1Ohy
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptgdstm1Ohy mutation (0 available); any Ptgds mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• homozygotes display no significant differences in general behavior or in the growth curves of body weight up to 40 weeks of age relative to wild-type littermates
• unlike in wild-type mice, where i.t. administration of PGE2 (10 ng/mouse) induces mechanical allodynic responses at 5 min after injection which gradually decrease over the 50-min experimental period, i.t. injection of PGE2 (10 ng) fails to induce any allodynia at the spinal level in homozygous mutant mice
• also unlike in wild-type mice, where i.t. administration of bicuculline (a GABA type A receptor antagonist, 25 ng/mouse) induces mechanical allodynia over a 50-min experiment, the bicuculline-evoked allodynic response of homozygous mutant mice is significantly reduced after the first 15 min and disappears thereafter
• while i.t. injection of PGD2 alone fails to induce allodynia in either wild-type or homozygous mutant mice at doses up to 100 ng, simultaneous injection of a femtogram amount of PGD2 with PGE2 or bicuculline induces allodynia in mutant mice to the same extent as in wild-type mice
• in addition, i.t. injection of PGF2alpha (1 g) induces allodynia for 50 min to a similar extent in wild-type and homozygous mutant mice

integument
N
• homozygotes show no significant differences in thermal hyperalgesia evoked by PGD2 and PGE2 at the spinal level, as determined by measuring the response time to a hot plate (55C) at 10 and 30 min after intrathecal (i.t.) injection of exogenous PGD2 (5 ng/mouse) and PGE2 (10 ng/mouse), respectively




Genotype
MGI:3700062
cx3
Allelic
Composition
ApcMin/Apc+
Ptgdstm1Ohy/Ptgdstm1Ohy
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (156 available)
Ptgdstm1Ohy mutation (0 available); any Ptgds mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice with Ptgds deficiency do not show altered adenoma profile compared to Apc heterozygous Ptgds-wild-type mice

digestive/alimentary system
• mice with Ptgds deficiency do not show altered adenoma profile compared to Apc heterozygous Ptgds-wild-type mice





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last database update
08/02/2024
MGI 6.24
The Jackson Laboratory