The LHX1 gene provides instructions for making a protein that attaches (binds) to specific regions of DNA and regulates the activity of other genes. On the basis of this role, the protein produced from the LHX1 gene is called a transcription factor. The LHX1 protein is part of a large group of transcription factors called homeodomain proteins. The homeodomain is a region of the protein that allows it to bind to DNA.
The LHX1 protein is found in many of the body's organs and tissues. Studies suggest that it plays particularly important roles in the development of the brain and female reproductive system.
Health Conditions Related to Genetic Changes
17q12 deletion syndrome
17q12 deletion syndrome is a condition that results from the deletion of a small piece of chromosome 17 in each cell. Signs and symptoms of 17q12 deletion syndrome can include abnormalities of the kidneys, urinary tract, and reproductive system; a form of diabetes called maturity-onset diabetes of the young type 5 (MODY5); delayed development; intellectual disability; and behavioral or psychiatric disorders. Some females with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by underdevelopment or absence of the vagina and uterus. Features associated with 17q12 deletion syndrome vary widely, even among affected members of the same family.
The part of chromosome 17 that is deleted is on the long (q) arm of the chromosome at a position designated q12. This region of the chromosome contains 15 genes, including LHX1. A deletion of this region results in a loss of one copy of the LHX1 gene in each cell, leading to a reduced amount of LHX1 protein. A shortage of this protein likely disrupts the regulation of genes that are necessary for the normal development of several organs, including the brain and female reproductive system. Researchers suspect that a loss of one copy of the LHX1 gene contributes to intellectual disability, behavioral and psychiatric conditions, and Mayer-Rokitansky-Küster-Hauser syndrome in people with 17q12 deletion syndrome.More About This Health Condition
MedlinePlus Genetics provides information about Mayer-Rokitansky-Küster-Hauser syndromeMore About This Health Condition
Other Names for This Gene
- homeobox protein Lim-1
- LIM homeobox protein 1
- LIM/homeobox protein Lhx1
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
- Hobert O, Westphal H. Functions of LIM-homeobox genes. Trends Genet. 2000 Feb;16(2):75-83. Review. Citation on PubMed
- Mefford HC, Clauin S, Sharp AJ, Moller RS, Ullmann R, Kapur R, Pinkel D, Cooper GM, Ventura M, Ropers HH, Tommerup N, Eichler EE, Bellanne-Chantelot C. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy. Am J Hum Genet. 2007 Nov;81(5):1057-69. Epub 2007 Sep 26. Citation on PubMed or Free article on PubMed Central
- Moreno-De-Luca D; SGENE Consortium, Mulle JG; Simons Simplex Collection Genetics Consortium, Kaminsky EB, Sanders SJ; GeneSTAR, Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, Morel CF, Boni C, Salbert BA, Chandrareddy A, Demmer LA, Chow EW, Surti U, Aradhya S, Pickering DL, Golden DM, Sanger WG, Aston E, Brothman AR, Gliem TJ, Thorland EC, Ackley T, Iyer R, Huang S, Barber JC, Crolla JA, Warren ST, Martin CL, Ledbetter DH. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet. 2010 Nov 12;87(5):618-30. doi: 10.1016/j.ajhg.2010.10.004. Epub 2010 Nov 4. Erratum in: Am J Hum Genet. 2011 Jan 7;88(1):121. Citation on PubMed or Free article on PubMed Central
- Nagamani SC, Erez A, Shen J, Li C, Roeder E, Cox S, Karaviti L, Pearson M, Kang SH, Sahoo T, Lalani SR, Stankiewicz P, Sutton VR, Cheung SW. Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12. Eur J Hum Genet. 2010 Mar;18(3):278-84. doi: 10.1038/ejhg.2009.174. Epub 2009 Oct 21. Citation on PubMed or Free article on PubMed Central