Stock

FESA Number

1589

Strain Name

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

Mutation Strain Type

Attribution

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.

Publications

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

Pages

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

EMMA ID

EM:01891

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