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

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 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

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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