PB 24168
Date
2004-03-26
Magnification
10x
Stain
HE
Author
helmholtz center munich, inst f radiation biology
Series
Description
Defect in Eye-lens development,
no lens induction at the placode stage,
mutation mapped to Mouse chromosome 19,
Marker intervall D19Mit21 - D19Mit10,
recessive transmission of phenotype,
complementation with Aphakia mutant
(Eyl-/- x Ak -/- F1 mice are affected),
Eyl-/- mice carry a frameshift mutation in Pitx3 gene
MPATH / Pathology
MPATH 86 - organ specific developmental defect
Gene
Pitx3
sex
Unknown
strain
C3H
organism
Mouse
EMAP / Embryonic stage, tissue or post-natal age:
EMAP 3980 - TS20,embryo
genotype status
Homozygous
genetic manipulation
Spontaneous-mutant
MA / Anatomical Site
MA 261 - eye
Designated Allele Name
Eyl
Experimental Manipulation
Further info
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