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 11 - 20 of 141 Stock Publications
Pubmed ID Authors Title Journal
11481423 Collinson JM Primary defects in the lens underlie complex anterior segment abnormalities of the Pax6 heterozygous eye. Proc Natl Acad Sci U S A (2 001) 98:9688-93
15142957 Funatsu N Gene expression analysis of the late embryonic mouse cerebral cortex using DNA microarray: identification of several region- and layer-specific genes. Cereb Cortex (2 004) 14:1031-44
1684639 Hill RE Mouse small eye results from mutations in a paired-like homeobox-containing gene. Nature (1 991) 354:522-5
24948600 Li X Sp8 plays a supplementary role to Pax6 in establishing the pMN/p3 domain boundary in the spinal cord. Development (2 014) 141:2875-84
11060242 Pratt T A role for Pax6 in the normal development of dorsal thalamus and its cortical connections. Development (2 000) 127:5167-78
11003833 Schwarz M Spatial specification of mammalian eye territories by reciprocal transcriptional repression of Pax2 and Pax6. Development (2 000) 127:4325-34
11003836 Toresson H Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2. Development (2 000) 127:4361-71
20040495 Zimmer C Role of Fgf8 signalling in the specification of rostral Cajal-Retzius cells. Development (2 010) 137:293-302
24290376 Bhatia S Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia. Am J Hum Genet (2 013) 93:1126-34
21309073 Compagnucci C Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center. Genesis (2 011) 49:307-25


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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