The human SHOX mutation database

Hum Mutat. 2002 Nov;20(5):338-41. doi: 10.1002/humu.10125.

Abstract

The human SHOX database has recently been established to provide clinicians and scientists access to a central source of information about all known SHOX mutations associated with short stature phenotypes such as idiopathic short stature, Lèri-Weill dyschondrosteosis, Langer syndrome, and Turner syndrome. So far, the database contains 29 unique intragenic mutations of the SHOX gene. These mutations were detected in a total of 39 patients from different families. Fourteen of these mutations have been found from the SHOX research group at the Institute of Human Genetics in Heidelberg, Germany; 25 mutations are from data reported in the literature. Not included in this database are complete SHOX gene deletions which represent the majority of all detectable SHOX mutations [Rappold et al., 2002]. The database is accessible via the website www.shox.uni-hd.de. It contains general information about the SHOX gene, and allows remote users to search the data and to submit new mutations to the database.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Databases, Nucleic Acid*
  • Genetic Diseases, Inborn / genetics
  • Homeodomain Proteins / genetics*
  • Humans
  • Internet
  • Molecular Sequence Data
  • Mutation*
  • Phenotype
  • Short Stature Homeobox Protein
  • Software

Substances

  • Homeodomain Proteins
  • SHOX protein, human
  • Short Stature Homeobox Protein

Associated data

  • GENBANK/U82668
  • OMIM/127300
  • OMIM/249700
  • OMIM/312865
  • OMIM/604271