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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rad23btm1Gvh
targeted mutation 1, Gijsbertus T J van der Horst
MGI:2179121
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rad23btm1Gvh/Rad23btm1Gvh involves: 129P2/OlaHsd * C57BL/6 MGI:2673543
cx2
Rad23atm1Jhjh/Rad23atm1Jhjh
Rad23btm1Gvh/Rad23b+
involves: 129P2/OlaHsd * C57BL/6 MGI:2672047
cx3
Rad23atm1Jhjh/Rad23a+
Rad23btm1Gvh/Rad23btm1Gvh
involves: 129P2/OlaHsd * C57BL/6 MGI:2672056
cx4
Rad23atm1Jhjh/Rad23atm1Jhjh
Rad23btm1Gvh/Rad23btm1Gvh
involves: 129P2/OlaHsd * C57BL/6 MGI:2672067


Genotype
MGI:2673543
hm1
Allelic
Composition
Rad23btm1Gvh/Rad23btm1Gvh
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rad23btm1Gvh mutation (0 available); any Rad23b mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• death between 0.5 and 1 year of age probably secondary to overall poor condition
• only 10% of expected numbers of homozygotes found at birth

behavior/neurological
• excessive washing activities
• involved head, ears, and neckline
• jumping (n=3)

cardiovascular system
• poor vascularization

craniofacial
• cleft lip is frequently seen in E13.5 to 19.5 embryos
• one instance of cleft secondary palate due to imperfect closure of the palatine shelves of the maxilla
• swelling of eyelids

digestive/alimentary system
• one instance of cleft secondary palate due to imperfect closure of the palatine shelves of the maxilla
• swollen anus
• soft oily feces

embryo
• vascular basement membrane was thicker and darker than normal
• swollen trophoblastic cells

endocrine/exocrine glands
• clusters of detatched sertioli cells found in the seminiferous tubules
• small diameter and with an excess of interstitial tissue

growth/size/body
• cleft lip is frequently seen in E13.5 to 19.5 embryos
• one instance of cleft secondary palate due to imperfect closure of the palatine shelves of the maxilla
• swelling of eyelids
• newborns much smaller than normal at birth and remain so throughout life
• growth retardation between E13.5 and 19.5

immune system

reproductive system
• clusters of detatched sertioli cells found in the seminiferous tubules
• small diameter and with an excess of interstitial tissue
• absent by day 15
• reduced female fertility although follicular development normal
• reduced female fertility although follicular development normal
• males are sterile

vision/eye
• animals avoid opening their eyes widely
• swelling of eyelids
• eyelids were not closed and fused as is normal between E15.5 and 19.5
• all other eye dysmorphology did not appear until 7 to 10 days of age
• some animals had "opaque eyes" but no further details were given
• excessive eye fluid starting at 7 to 10 days of age

adipose tissue
• adults lack fatty tissue

homeostasis/metabolism
• swelling of eyelids

integument




Genotype
MGI:2672047
cx2
Allelic
Composition
Rad23atm1Jhjh/Rad23atm1Jhjh
Rad23btm1Gvh/Rad23b+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rad23atm1Jhjh mutation (0 available); any Rad23a mutation (12 available)
Rad23btm1Gvh mutation (0 available); any Rad23b mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:2672056
cx3
Allelic
Composition
Rad23atm1Jhjh/Rad23a+
Rad23btm1Gvh/Rad23btm1Gvh
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rad23atm1Jhjh mutation (0 available); any Rad23a mutation (12 available)
Rad23btm1Gvh mutation (0 available); any Rad23b mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• however, cells are capable of nucleotide excision repair
• embryos survive at least through E13.5 when mouse embryo fibroblasts were isolated




Genotype
MGI:2672067
cx4
Allelic
Composition
Rad23atm1Jhjh/Rad23atm1Jhjh
Rad23btm1Gvh/Rad23btm1Gvh
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rad23atm1Jhjh mutation (0 available); any Rad23a mutation (12 available)
Rad23btm1Gvh mutation (0 available); any Rad23b mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die sometime between E8.5 and E10.5

cellular
• embryos are deficient in nucleotide excision repair

homeostasis/metabolism
• embryos are deficient in nucleotide excision repair





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory