Related Experiment Video
Updated: Aug 16, 2026

Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation
N K Ragge1, A Salt, J R O Collin
1Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK. nicky.ragge@anat.ox.ac.uk
Aim:
To identify a gene linking microphthalmia with cyst with early onset medulloblastoma.
Methods:
Mutation analysis of the PTCH gene.
Results:
A mutation in exon 10 of the PTCH gene was identified, confirming a diagnosis of Gorlin syndrome.
Conclusions:
This is the first genetically identified mutation giving rise to microphthalmia with cyst and provides a valuable link in the eye developmental gene pathway.
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