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 101 - 110 of 141 Stock Publications
Pubmed ID Authors Title Journal
10772788 Enwright JF 3rd Altered retinoid signaling in the heads of small eye mouse embryos. Dev Biol (2 000) 221:10-22
9636075 Hallonet M Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrain. Development (1 998) 125:2599-610
15917450 Kimura J Emx2 and Pax6 function in cooperation with Otx2 and Otx1 to develop caudal forebrain primordium that includes future archipallium. J Neurosci (2 005) 25:5097-108
12764040 Muzio L Emx1, emx2 and pax6 in specification, regionalization and arealization of the cerebral cortex. Cereb Cortex (2 003) 13:641-7
19521500 Sansom SN The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis. PLoS Genet (2 009) 5:e1000511
9828088 Sun T Pax6 influences the time and site of origin of glial precursors in the ventral neural tube. Mol Cell Neurosci (1 998) 12:228-39
23404109 Walcher T Functional dissection of the paired domain of Pax6 reveals molecular mechanisms of coordinating neurogenesis and proliferation. Development (2 013) 140:1123-36
8801186 West JD A quantitative test for developmental neutrality of a transgenic lineage marker in mouse chimaeras. Genet Res (1 996) 67:135-46
Clayton RM Pax6<Sey> - small eye Mouse News Lett (1 968) 39:22
11807037 Estivill-Torrus G Pax6 is required to regulate the cell cycle and the rate of progression from symmetrical to asymmetrical division in mammalian cortical progenitors. Development (2 002) 129:455-66


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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