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 61 - 70 of 141 Stock Publications
Pubmed ID Authors Title Journal
12514213 Stenman J Identification of two distinct progenitor populations in the lateral ganglionic eminence: implications for striatal and olfactory bulb neurogenesis. J Neurosci (2 003) 23:167-74
17953485 Visel A Regulatory pathway analysis by high-throughput in situ hybridization. PLoS Genet (2 007) 3:1867-83
3733894 Lo CW Localization of low abundance DNA sequences in tissue sections by in situ hybridization. J Cell Sci (1 986) 81:143-62
9362466 Cari? D Determination of the migratory capacity of embryonic cortical cells lacking the transcription factor Pax-6. Development (1 997) 124:5087-96
9853907 Dellovade TL Olfactory bulb development is altered in small-eye (Sey) mice. J Comp Neurol (1 998) 402:402-18
9856459 Götz M Pax6 controls radial glia differentiation in the cerebral cortex. Neuron (1 998) 21:1031-44
11731698 Jaskoll T Embryonic submandibular gland morphogenesis: stage-specific protein localization of FGFs, BMPs, Pax6 and Pax9 in normal mice and abnormal SMG phenotypes in FgfR2-IIIc(+/Delta), BMP7(-/-) and Pax6(-/-) mice. Cells Tissues Organs (2 002) 170:83-98
21205789 Matsushima D Combinatorial regulation of optic cup progenitor cell fate by SOX2 and PAX6. Development (2 011) 138:443-54
8600027 Quinn JC Multiple functions for Pax6 in mouse eye and nasal development. Genes Dev (1 996) 10:435-46
12764029 Stoykova A Increase in reelin-positive cells in the marginal zone of Pax6 mutant mouse cortex. Cereb Cortex (2 003) 13:560-71


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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