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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