About   Help   FAQ
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 (34 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 (34 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory