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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ripply3tm1Sjt
targeted mutation 1, Shinji Takada
MGI:4880754
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ripply3tm1Sjt/Ripply3tm1Sjt involves: 129S1/Sv * C57BL/6 MGI:4880755
cx2
Ripply3tm1Sjt/Ripply3tm1Sjt
Tbx1tm1Bem/Tbx1tm1Bem
involves: 129/Sv * 129S1/Sv * C57BL/6J * SJL MGI:4880757
cx3
Ripply3tm1Sjt/Ripply3+
Tbx1tm1Bem/Tbx1+
involves: 129/Sv * 129S1/Sv * C57BL/6J * SJL MGI:4880759


Genotype
MGI:4880755
hm1
Allelic
Composition
Ripply3tm1Sjt/Ripply3tm1Sjt
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ripply3tm1Sjt mutation (0 available); any Ripply3 mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

homeostasis/metabolism

embryo
• abnormally persistent and remains connected to the dorsal aorta at E10.5
• neural crest cells fail to populate the third and fourth pharyngeal arches
• severely reduced in size at E9.5 and E10.5
• the ectoderm and endoderm layers are adjacent
• unidentifiable at E10.5
• severely reduced in size at E9.5 and E10.5
• the ectoderm and endoderm layers are adjacent
• unidentifiable at E10.5
• severe reduction in the size of the third and fourth arches at E9.5 and E10.5
• dramatic increase in apoptosis in the caudal pharyngeal region
• neural crest cells fail to populate the third and fourth pharyngeal arches
• lack the characteristic segmental pattern in the caudal arches
• defects in the development of tissues derived from the third and fourth pharyngeal pouches characterized by failure of the primordia to separate from the pouch
• no obvious abnormalities are seen in derivatives of the first and second pouches
• at E13.5 expression analysis indicates that the primordia of the ultimobranchial bodies fail to separate from the epithelium in the pharyngeal pouch

cardiovascular system
• two additional ascending arteries are ectopically formed to the common carotid arteries
• unidentifiable at E10.5
• abnormally persistent and remains connected to the dorsal aorta at E10.5
• unidentifiable at E10.5
• hypotrophic in the conotruncus region
• abnormally branch from the dorsal aorta in the retroesophageal region
• abnormal persistence and regression of the branchial arch arteries
• persists and anastomoses with the descending dorsal aorta
• incomplete formation of the ventricular septum

endocrine/exocrine glands
• at E13.5 expression analysis indicates that the primordia of the ultimobranchial bodies fail to separate from the epithelium in the pharyngeal pouch
• increase in alpha cell area
• increase in beta cell area
• at E13.5 expression analysis indicates that the parathyroid gland primordia fail to detach from the endodermal epithelium and are smaller than normal
• at E13.5 expression analysis indicates the thymus is formed but fails to separate from the pharyngeal endoderm
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• in many cases, the ectopic thymus appears to have evaginated into the oropharynx

hematopoietic system
• at E13.5 expression analysis indicates the thymus is formed but fails to separate from the pharyngeal endoderm
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• in many cases, the ectopic thymus appears to have evaginated into the oropharynx

immune system
• at E13.5 expression analysis indicates the thymus is formed but fails to separate from the pharyngeal endoderm
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• at E18.5 the thymus fails to migrate caudally and is present ectopically in the pharynx region
• in many cases, the ectopic thymus appears to have evaginated into the oropharynx

craniofacial
• abnormally persistent and remains connected to the dorsal aorta at E10.5
• severely reduced in size at E9.5 and E10.5
• the ectoderm and endoderm layers are adjacent
• unidentifiable at E10.5
• severely reduced in size at E9.5 and E10.5
• the ectoderm and endoderm layers are adjacent
• unidentifiable at E10.5
• severe reduction in the size of the third and fourth arches at E9.5 and E10.5

cellular
• abnormal persistence and regression of the branchial arch arteries
• neural crest cells fail to populate the third and fourth pharyngeal arches




Genotype
MGI:4880757
cx2
Allelic
Composition
Ripply3tm1Sjt/Ripply3tm1Sjt
Tbx1tm1Bem/Tbx1tm1Bem
Genetic
Background
involves: 129/Sv * 129S1/Sv * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ripply3tm1Sjt mutation (0 available); any Ripply3 mutation (9 available)
Tbx1tm1Bem mutation (1 available); any Tbx1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• absent in the caudal branchial region

cardiovascular system
• at E18.5 the phenotype is identical to mice homozygous null for Tbx1 alone




Genotype
MGI:4880759
cx3
Allelic
Composition
Ripply3tm1Sjt/Ripply3+
Tbx1tm1Bem/Tbx1+
Genetic
Background
involves: 129/Sv * 129S1/Sv * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ripply3tm1Sjt mutation (0 available); any Ripply3 mutation (9 available)
Tbx1tm1Bem mutation (1 available); any Tbx1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• hypotrophic fourth arch at E10.5

craniofacial
• hypotrophic fourth arch at E10.5





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory