Stock

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 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

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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