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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ror2Y324C
Tyr324Cys
MGI:5305088
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ror2Y324C/Ror2Y324C involves: C57BL/6J MGI:5305090
cx2
Baxtm1Sjk/Baxtm1Sjk
Ror2Y324C/Ror2Y324C
involves: 129X1/SvJ * C57BL/6J MGI:5305092


Genotype
MGI:5305090
hm1
Allelic
Composition
Ror2Y324C/Ror2Y324C
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ror2Y324C mutation (0 available); any Ror2 mutation (125 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Ror2Y324C/Ror2Y324C and Ror2tm1Ymi/Ror2tm1Ymi mice exhibit short tails at E10.75

mortality/aging

reproductive system
• total numbers and the number in the gonads are decreased at E11.5 and E12.5, but not at E10.5
• cultured primordial germ cells show impaired elongation and alignment along an SCF (secreted Kit ligand) gradient
• increase in apoptosis of extragonadal primordial germ cells at E10.5 and E11.5
• ectopic PGCs are seen in the allantois, throughout the tail mesoderm, and caudal hindgut at E9.0
• fail to migrate rostrally at E10.5, remaining in the mesentery surrounding the caudal hindgut as well as on the surface of the tail and in the allantois
• at E11.5 the distribution of PGCs is skewed toward the caudal end of the gonad and an increased number of extragonadal PGCs are present in midline tissues
• ectopic PGCs make up 30% of the total PGCs at E11.5 compared to less than 5% in wild-type controls
• cell elongation of migratory PGCs is impaired at E9.75-E10.75

digestive/alimentary system
• wider and shorter caudal hindgut at E9.5

limbs/digits/tail
• defects in tail elongation

embryo
• defects in somite segmentation

cellular
• total numbers and the number in the gonads are decreased at E11.5 and E12.5, but not at E10.5
• increase in apoptosis of extragonadal primordial germ cells at E10.5 and E11.5
• ectopic PGCs are seen in the allantois, throughout the tail mesoderm, and caudal hindgut at E9.0
• fail to migrate rostrally at E10.5, remaining in the mesentery surrounding the caudal hindgut as well as on the surface of the tail and in the allantois
• at E11.5 the distribution of PGCs is skewed toward the caudal end of the gonad and an increased number of extragonadal PGCs are present in midline tissues
• ectopic PGCs make up 30% of the total PGCs at E11.5 compared to less than 5% in wild-type controls
• cell elongation of migratory PGCs is impaired at E9.75-E10.75




Genotype
MGI:5305092
cx2
Allelic
Composition
Baxtm1Sjk/Baxtm1Sjk
Ror2Y324C/Ror2Y324C
Genetic
Background
involves: 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Baxtm1Sjk mutation (1 available); any Bax mutation (24 available)
Ror2Y324C mutation (0 available); any Ror2 mutation (125 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• no increase in the number of gonadal PGCs is seen compared to mutant mice wild-type for Bax
• increase in the number of ectopic PGCs compared to mutant mice wild-type for Bax

cellular
• no increase in the number of gonadal PGCs is seen compared to mutant mice wild-type for Bax
• increase in the number of ectopic PGCs compared to mutant mice wild-type for Bax





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory