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 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

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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