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 51 - 60 of 141 Stock Publications
Pubmed ID Authors Title Journal
9363853 Quinn JC Genetic background effects on dental and other craniofacial abnormalities in homozygous small eye (Pax6Sey/Pax6Sey) mice. Anat Embryol (Berl) (1 997) 196:311-21
12571103 Stenman J Tlx and Pax6 co-operate genetically to establish the pallio-subpallial boundary in the embryonic mouse telencephalon. Development (2 003) 130:1113-22
11076764 van Raamsdonk CD Dosage requirement and allelic expression of PAX6 during lens placode formation. Development (2 000) 127:5439-48
3428512 Lo CW Tracking of mouse cell lineage using microinjected DNA sequences: analyses using genomic Southern blotting and tissue-section in situ hybridizations. Differentiation (1 987) 35:37-44
9733944 Brunjes PC The small-eye mutation results in abnormalities in the lateral cortical migratory stream. Brain Res Dev Brain Res (1 998) 110:121-5
9593910 Dellovade TL The gonadotropin-releasing hormone system does not develop in Small-Eye (Sey) mouse phenotype. Brain Res Dev Brain Res (1 998) 107:233-40
16525473 Gosgnach S V1 spinal neurons regulate the speed of vertebrate locomotor outputs. Nature (2 006) 440:215-9
17900924 Hufnagel RB Conserved regulation of Math5 and Math1 revealed by Math5-GFP transgenes. Mol Cell Neurosci (2 007) 36:435-48
22581784 Matsumata M The effects of Fabp7 and Fabp5 on postnatal hippocampal neurogenesis in the mouse. Stem Cells (2 012) 30:1532-43
16979618 Quinn JC Pax6 controls cerebral cortical cell number by regulating exit from the cell cycle and specifies cortical cell identity by a cell autonomous mechanism. Dev Biol (2 007) 302:50-65


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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