Phenotype: Leri-Weill dyschondrosteosis


OMIM: 127300
Inheritance: Autosomal dominant
Classification: Congenital malformations, deformations and chromosomal abnormalities

Related informations: Gene Tests    Clinical Synopsis    Clinical Trials

SHOX || c.508G>C

Gene/Locus:    SHOX
Dna Change:    c.508G>C
Protein Change:    p.Ala170Pro
Mutation Type:    Substitution
Mutation Effect:    Missense
Location:    exon 4
Transcript:    NM_000451.3

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
ItalyGypsyNANANABarca-Tierno V et al., 2011Barca-Tierno V, Aza-Carmona M, Barroso E, Heine-Suner D, Azmanov D, Rosell J, Ezquieta B, Montané LS, Vendrell T, Cruz J, Santos F, Rodríguez JI, Pozo J, Argente J, Kalaydjieva L, Gracía R, Campos-Barros A, Benito-Sanz S, Heath KE, . Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia.. Eur. J. Hum. Genet.. 2011; 19(12):1218-25

References

Barca-Tierno V, Aza-Carmona M, Barroso E, Heine-Suner D, Azmanov D, Rosell J, Ezquieta B, Montané LS, Vendrell T, Cruz J, Santos F, Rodríguez JI, Pozo J, Argente J, Kalaydjieva L, Gracía R, Campos-Barros A, Benito-Sanz S, Heath KE, Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia.Eur. J. Hum. Genet.. 2011; 19(12):1218-25