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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rxfp2tm1Aia
targeted mutation 1, Alexander I Agoulnik
MGI:2388129
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rxfp2tm1Aia/Rxfp2tm1Aia involves: 129S7/SvEvBrd MGI:5473316
hm2
Rxfp2tm1Aia/Rxfp2tm1Aia involves: 129S7/SvEvBrd * C57BL/6J MGI:2388134
cn3
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Rarb-cre)1Bhr/0
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6N * SJL MGI:5473318
cn4
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Tagln-cre)1Her/0
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6N * SJL MGI:5473320
cn5
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(ACTA1-cre)79Jme/0
involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N * SJL MGI:5473317
cn6
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Stra8-icre)1Reb/0
involves: 129S7/SvEvBrd * C57BL/6N * FVB/NJ MGI:5473319
cx7
Rxfp1tm1Aia/Rxfp1tm1Aia
Rxfp2tm1Aia/Rxfp2tm1Aia
involves: 129S7/SvEvBrd * C57BL/6J MGI:3054971
cx8
Cav1tm1.1Aia/Cav1tm1.1Aia
Rxfp2tm1Aia/Rxfp2+
involves: 129S7/SvEvBrd * C57BL/6J * FVB MGI:5141501
cx9
Rxfp2tm1Aia/crsp involves: 129S7/SvEvBrd * C57BL/6J * FVB/N MGI:3603529


Genotype
MGI:5473316
hm1
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1Aia
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• high intra-abdominal cryptorchidism

reproductive system
• high intra-abdominal cryptorchidism




Genotype
MGI:2388134
hm2
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1Aia
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• absence of spermatids and mature sperm

reproductive system
• absence of spermatids and mature sperm
• bilaterally undescended testis located in the high intraabdominal position
• extended gubernaculum
• inguinal canal fails to form

endocrine/exocrine glands
• bilaterally undescended testis located in the high intraabdominal position

skeleton
• extended gubernaculum

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cryptorchidism DOID:11383 OMIM:219050
J:79124




Genotype
MGI:5473318
cn3
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Rarb-cre)1Bhr/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
Rxfp2tm1c(EUCOMM)Wtsi mutation (0 available); any Rxfp2 mutation (53 available)
Tg(Rarb-cre)1Bhr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• high intra-abdominal cryptorchidism

endocrine/exocrine glands
• high intra-abdominal cryptorchidism




Genotype
MGI:5473320
cn4
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Tagln-cre)1Her/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
Rxfp2tm1c(EUCOMM)Wtsi mutation (0 available); any Rxfp2 mutation (53 available)
Tg(Tagln-cre)1Her mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• mice exhibit normal testis position




Genotype
MGI:5473317
cn5
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(ACTA1-cre)79Jme/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
Rxfp2tm1c(EUCOMM)Wtsi mutation (0 available); any Rxfp2 mutation (53 available)
Tg(ACTA1-cre)79Jme mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• mice exhibit normal testis position




Genotype
MGI:5473319
cn6
Allelic
Composition
Rxfp2tm1Aia/Rxfp2tm1c(EUCOMM)Wtsi
Tg(Stra8-icre)1Reb/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6N * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
Rxfp2tm1c(EUCOMM)Wtsi mutation (0 available); any Rxfp2 mutation (53 available)
Tg(Stra8-icre)1Reb mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• mice exhibit normal reproductive organ abnormalities




Genotype
MGI:3054971
cx7
Allelic
Composition
Rxfp1tm1Aia/Rxfp1tm1Aia
Rxfp2tm1Aia/Rxfp2tm1Aia
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rxfp1tm1Aia mutation (0 available); any Rxfp1 mutation (53 available)
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• mutant females have small nipples
• intra-abdominal cryptorchism is seen
• 1 male (out of 11) showed unilateral torsion of the cryptorchid testis with hemorrhage and necrosis and 2 others were missing the right testis probably as a result of necrosis following torsion
• about 2/3 of the mutant females are unable to nurse pups

reproductive system
• intra-abdominal cryptorchism is seen
• 1 male (out of 11) showed unilateral torsion of the cryptorchid testis with hemorrhage and necrosis and 2 others were missing the right testis probably as a result of necrosis following torsion

respiratory system
N
• no significant fibrosis is seen in the lungs

integument
• mutant females have small nipples
• about 2/3 of the mutant females are unable to nurse pups




Genotype
MGI:5141501
cx8
Allelic
Composition
Cav1tm1.1Aia/Cav1tm1.1Aia
Rxfp2tm1Aia/Rxfp2+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cav1tm1.1Aia mutation (0 available); any Cav1 mutation (29 available)
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• female mice are fertile
• mice exhibit an increase in the number of endometrial glands compared with wild-type mice
• in 6% of mice at 11 to 13 months
• in 24% of mice at 5 to 7 months
• in 58% of mice at 11 to 13 months
• endometrial glandular epithelium in mice with cysts exhibit increased proliferation compared to in wild-type mice

neoplasm
N
• mice do not develop endometrial cancer or metastases

endocrine/exocrine glands
• mice exhibit an increase in the number of endometrial glands compared with wild-type mice
• in 6% of mice at 11 to 13 months

growth/size/body
• in 6% of mice at 11 to 13 months
• in 24% of mice at 5 to 7 months
• in 58% of mice at 11 to 13 months




Genotype
MGI:3603529
cx9
Allelic
Composition
Rxfp2tm1Aia/crsp
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
crsp mutation (0 available); any crsp mutation (0 available)
Rxfp2tm1Aia mutation (0 available); any Rxfp2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• absence of spermatids and mature sperm

reproductive system
• absence of spermatids and mature sperm
• bilaterally undescended testis located in the high intraabdominal position
• extended gubernaculum
• inguinal canal fails to form

endocrine/exocrine glands
• bilaterally undescended testis located in the high intraabdominal position

skeleton
• extended gubernaculum

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cryptorchidism DOID:11383 OMIM:219050
J:79124





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory