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 131 - 140 of 141 Stock Publications
Pubmed ID Authors Title Journal
8689689 Schedl A Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities. Cell (1 996) 86:71-82
11493521 Tarabykin V Cortical upper layer neurons derive from the subventricular zone as indicated by Svet1 gene expression. Development (2 001) 128:1983-93
24698273 Zhang J V1 and v2b interneurons secure the alternating flexor-extensor motor activity mice require for limbed locomotion. Neuron (2 014) 82:138-50
10662634 Collinson JM Different roles for Pax6 in the optic vesicle and facial epithelium mediate early morphogenesis of the murine eye. Development (2 000) 127:945-56
18700968 Fotaki V Newly identified patterns of Pax2 expression in the developing mouse forebrain. BMC Dev Biol (2 008) 8:79
15031110 Heller RS The role of Brn4/Pou3f4 and Pax6 in forming the pancreatic glucagon cell identity. Dev Biol (2 004) 268:123-34
16364898 Landsberg RL Hindbrain rhombic lip is comprised of discrete progenitor cell populations allocated by Pax6. Neuron (2 005) 48:933-47
24814534 Pattabiraman K Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortex. Neuron (2 014) 82:989-1003
8213068 Schmahl W Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus. Acta Neuropathol (1 993) 86:126-35
15758185 Tole S Selective requirement of Pax6, but not Emx2, in the specification and development of several nuclei of the amygdaloid complex. J Neurosci (2 005) 25:2753-60


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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