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Phenotypes Associated with This Genotype
Genotype
MGI:3580500
Allelic
Composition
Lhx1tm2.1Bhr/Lhx1tm1Tmj
Tg(Hoxb7-cre)13Amc/0
Genetic
Background
involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lhx1tm1Tmj mutation (0 available); any Lhx1 mutation (22 available)
Lhx1tm2.1Bhr mutation (0 available); any Lhx1 mutation (22 available)
Tg(Hoxb7-cre)13Amc mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• hypoplastic metanephroi with reduced number of glomeruli
• however, morphologically normal medulla and glomeruli
• neonates had small metanephroi that were functional at birth
• observed in 40% of mutants
• greatly reduced numbers of developing nephrons at birth
• the distal ureter was closed in both sexes
• the distal ureter ended abnormally in the uterus in some females
• observed in 40% of mutants
• delayed induction of the ureteric bud

reproductive system
• 57.1% of mutant females had completely or partially absent uteri with residual uterine tissue discontinuously present
• posterior uterus was more frequently absent compared to the anterior region
• 57.1% of mutant females had completely or partially absent uteri
• absent epididymis in all mutant males

embryo
• loss of caudal mesonephric tubules; however, the cranial mesonephros was present
• exhibited Mullerian duct aplasia, impaired posterior elongation of the Mullerian duct and Mullerian duct degeneration adjacent to where the Wolffian duct was lost
• degeneration of the nephric (Wolffian) duct epithelium that resulted in the absence of most parts of the reproductive tract in all mutant males, except for some residual tissue


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