GPC3
Gene name: glypican 3OMIM ID: 300037
Chromosome location: Xq26.2
Mutations
Disease/Phenotype | Simpson-Golabi-Behmel syndrome, type 1 (SGBS) |
---|---|
Reference transcript | NM_001164617.1 |
DNA Change | c.271C>T |
A.A. Change | p.GLn91X |
Exon/Intron | exon 2 |
Mutation Type | substitution |
Reference | Ratbi I, Elalaoui SC, Moizard MP, Raynaud M, Sefiani A.Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome. Turk J Pediatr. 2010 Sep-Oct;52(5):525-8. |