Stock 129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

FESA Number


Strain Name

129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

Mutation Strain Type


Gene/Allele Information

Allele Name Allele MGI ID Gene Name Gene MGI ID Chromosome
Pax6<Sey> MGI:1856155 Pax6 MGI:97490 2
Tg(Hbb-b1)83Clo MGI:2655271 3

Phenotypic Description

Reiterated transgene is detectable by DNA in situ hybridisation.


Displaying 41 - 50 of 141 Stock Publications
Pubmed ID Authors Title Journal
17202185 Manuel M Controlled overexpression of Pax6 in vivo negatively autoregulates the Pax6 locus, causing cell-autonomous defects of late cortical progenitor proliferation with little effect on cortical arealization. Development (2 007) 134:545-55
16024294 Purcell P Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction. Gene Expr Patterns (2 005) 6:110-8
17428831 Song N pygopus 2 has a crucial, Wnt pathway-independent function in lens induction. Development (2 007) 134:1873-85
17721516 Uemura M OL-Protocadherin is essential for growth of striatal axons and thalamocortical projections. Nat Neurosci (2 007) 10:1151-9
12846477 Keighren MA Polyploid cells in the mouse ovary. J Anat (2 003) 202:563-71
9806930 Brown NL Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis. Development (1 998) 125:4821-33
7649798 Dangata YY Morphometric study of the optic nerve of adult normal mice and mice heterozygous for the Small eye mutation (Sey/+). J Anat (1 994) 185 ( Pt 3):627-35
17634386 Gopal PP Pax6-/- mice have a cell nonautonomous defect in nonradial interneuron migration. Cereb Cortex (2 008) 18:752-62
17158062 Holm PC Loss- and gain-of-function analyses reveal targets of Pax6 in the developing mouse telencephalon. Mol Cell Neurosci (2 007) 34:99-119
9169845 Mastick GS Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain. Development (1 997) 124:1985-97


Orphanet Categories

Rare developmental defect during embryogenesis
Rare urogenital disease
Rare renal disease
Rare eye disease
Rare endocrine disease
Rare oncologic disease
Rare gynecologic or obstetric disease
Rare neurologic disease




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