Possible linkage of non-syndromic cleft lip and palate to the MSX1 homebox gene on chromosome 4p

Journal Article · Thu Sep 01 00:00:00 EDT 1994 · American Journal of Human Genetics

OSTI ID:134730

Wang, S; Walczak, C; Erickson, R P

The MSX1 (HOX7) gene has been shown recently to cause cleft palate in a mouse model deficient for its product. Several features of this mouse model make the human homolog of this gene an excellent candidate for non-syndromic cleft palate. We tested this hypothesis by linkage studies in two large multiplex human families using a microsatellite marker in the human MSX1 gene. A LOD score of 1.7 was obtained maximizing at a recombination fraction of 0.09. Computer simulation power calculations using the program SIMLINK indicated that a LOD score this large is expected to occur only about 1/200 times by chance alone for a marker locus with comparable informativeness if unlinked to the disease gene. This suggestive finding is being followed up by attempts to recruit and study additional families and by DNA sequence analyses of the MSX1 gene in these families and other cleft lip and/or cleft palate subjects and these further results will also be reported.

• OSTI ID: 134730
• Report Number(s): CONF-941009-; ISSN 0002-9297; TRN: 95:005313-1468
• Journal Information: American Journal of Human Genetics, Vol. 55, Issue Suppl.3; Conference: 44. annual meeting of the American Society of Human Genetics, Montreal (Canada), 18-22 Oct 1994; Other Information: PBD: Sep 1994
• Country of Publication: United States
• Language: English

Related Subjects

55 BIOLOGY AND MEDICINE
BASIC STUDIES
99 MATHEMATICS
COMPUTERS
INFORMATION SCIENCE
MANAGEMENT
LAW
MISCELLANEOUS
PATIENTS
HEREDITARY DISEASES
CONGENITAL MALFORMATIONS
GENES
GENETIC MAPPING
DNA SEQUENCING
HUMAN CHROMOSOMES
S CODES
COMPUTERIZED SIMULATION
BIOLOGICAL MODELS
BIOLOGICAL MARKERS
GENETICS
MICE