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 121 - 130 of 141 Stock Publications
Pubmed ID Authors Title Journal
25936505 Kong JH Notch activity modulates the responsiveness of neural progenitors to sonic hedgehog signaling. Dev Cell (2 015) 33:373-87
18371392 Nikoletopoulou V Neurotrophin receptor-mediated death of misspecified neurons generated from embryonic stem cells lacking Pax6. Cell Stem Cell (2 007) 1:529-40
11502253 Scardigli R Crossregulation between Neurogenin2 and pathways specifying neuronal identity in the spinal cord. Neuron (2 001) 31:203-17
21625468 Szabó NE Interaction between axons and specific populations of surrounding cells is indispensable for collateral formation in the mammillary system. PLoS One (2 011) 6:e20315
9108373 Warren N Roles of Pax-6 in murine diencephalic development. Development (1 997) 124:1573-82
12648492 Collinson JM The roles of Pax6 in the cornea, retina, and olfactory epithelium of the developing mouse embryo. Dev Biol (2 003) 255:303-12
18165280 Faedo A COUP-TFI coordinates cortical patterning, neurogenesis, and laminar fate and modulates MAPK/ERK, AKT, and beta-catenin signaling. Cereb Cortex (2 008) 18:2117-31
11896398 Heins N Glial cells generate neurons: the role of the transcription factor Pax6. Nat Neurosci (2 002) 5:308-15
15878992 Kroll TT Ventralized dorsal telencephalic progenitors in Pax6 mutant mice generate GABA interneurons of a lateral ganglionic eminence fate. Proc Natl Acad Sci U S A (2 005) 102:7374-9
20844123 Panayi H Sox1 is required for the specification of a novel p2-derived interneuron subtype in the mouse ventral spinal cord. J Neurosci (2 010) 30:12274-80


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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