T-box genes in human disorders

Hum Mol Genet. 2003 Apr 1:12 Spec No 1:R37-44. doi: 10.1093/hmg/ddg077.

Abstract

The T-box gene family encodes a large family of transcription factors with more than 20 members identified in humans so far, and homologues in many other organisms. A number of human disorders have been linked to mutations in T-box genes, confirming their medical importance. They include Holt- Oram syndrome/TBX5, Ulnar-Mammary syndrome/TBX3, and more recently DiGeorge syndrome/TBX1, ACTH deficiency/TBX19 and cleft palate with ankyloglossia/TBX22. This review describes the key features of these disorders and the involvement of T-box genes in their phenotype.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adrenocorticotropic Hormone / deficiency
  • Animals
  • Bone and Bones
  • DiGeorge Syndrome / genetics
  • Humans
  • Mice
  • Models, Genetic
  • Mutation
  • Phenotype
  • Syndrome
  • T-Box Domain Proteins / genetics*
  • T-Box Domain Proteins / metabolism
  • T-Box Domain Proteins / physiology*
  • X-Rays

Substances

  • T-Box Domain Proteins
  • Adrenocorticotropic Hormone

Associated data

  • OMIM/102150
  • OMIM/188400
  • OMIM/303400