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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rfx2Gt(IST10638H11)Tigm
gene trap IST10638H11, Texas A&M Institute for Genomic Medicine
MGI:3966900
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rfx2Gt(IST10638H11)Tigm/Rfx2Gt(IST10638H11)Tigm either: C57BL/6N-Rfx2Gt(IST10638H11)Tigm or (involves: C57BL/6N * CD-1) MGI:5705076


Genotype
MGI:5705076
hm1
Allelic
Composition
Rfx2Gt(IST10638H11)Tigm/Rfx2Gt(IST10638H11)Tigm
Genetic
Background
either: C57BL/6N-Rfx2Gt(IST10638H11)Tigm or (involves: C57BL/6N * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rfx2Gt(IST10638H11)Tigm mutation (1 available); any Rfx2 mutation (79 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

In Rfx2Gt(IST10638H11)Tigm/Rfx2Gt(IST10638H11)Tigm testis, elongating spermatids are replaced by symblasts of spermatids

cellular
• elongating spermatids are replaced by symplasts of spermatids
• an accumulation of abnormal symplasts of round spermatids is observed
• an accumulation of abnormal symplasts of round spermatids is observed

reproductive system
• an accumulation of abnormal symplasts of round spermatids is observed
• Leydig cells appear enlarged
• increased numbers of Leydig cells are present in the interstitial space
• no sperm is recovered from the caudal epididymis at 12 weeks of age
• no spermatozoa are present in the lumen of seminiferous tubules
• however, spermatogonial cells and spermatocytes are present in mutant testes and do not appear obviously abnormal
• elongating spermatids are replaced by symplasts of spermatids
• an accumulation of abnormal symplasts of round spermatids is observed
• differentiation of spermatids is abnormal before or at the round and elongating spermatid stage
• male homozygotes are infertile despite normal mating and plugging behavior
• in contrast, female homozygotes are fertile

endocrine/exocrine glands
• Leydig cells appear enlarged
• increased numbers of Leydig cells are present in the interstitial space

embryo
N
• homozygotes appear morphologically normal at E10.5
• no defects in neural tube closure or in organ situs (left-right patterning) are observed

behavior/neurological
N
• adult homozygotes are viable, morphologically normal, and do not exhibit any obvious behavioral abnormalities





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory