
Entry - *603202 - LACTASE; LCT - OMIM
2008年2月26日 · Kruse et al. (1989) studied linkage of a RFLP associated with the lactase-phlorizin hydrolase gene (which they symbolized LPH) to multiple genetic markers from chromosome 2 and found linkage to 2 of them. Harvey et al. (1993) described the regional localization of LCT to 2q21 by PCR analysis of somatic cell hybrids and by in situ hybridization ...
The lactase phlorizin hydrolase (LCT) gene maps to pig
A porcine 17kb genomic fragment was used as probe to map the lactase phlorizin hydrolase (LCT) gene to pig chromosome 15q13 by fluorescence in situ hybridization. Further, a three-allele TaqI RFLP was used to add the LCT gene to the proximal end of …
Analysis of a SNP linked to lactase persistence: An exercise for ...
2011年3月28日 · If a person was suffering from gastrointestinal disturbances but was of the genotype −13,910 C/T or −13,910 T/T then lactose intolerance could most likely be eliminated as the cause. In fact, PCR-RFLP genotyping and polymerase chain reaction minisequencing assays have been developed by other labs for this purpose [13, 14].
The lactase persistence allele –22018 G/A associated
2020年6月1日 · Lactase persistence (LP; OMIM # 223100) is the ability to digest milk sugar in adulthood (Ingram et al., 2009). Intestinal lactase activity is regulated by cis -acting elements of the lactase gene (LCT; OMIM *603202), which has …
Restriction fragment length polymorphism (RFLP) and
The lactase persistent (LP) or lactase non-persistent (LNP) state in European adults is genetically determined by a single nucleotide polymorphism (SNP) located 13.9 kb...
The influence of host genetics on the microbiome - PMC
The earliest attempts to understand microbiome assembly used gel electrophoresis–based community fingerprinting methods, such as terminal-restriction fragment length polymorphism (T-RFLP) analysis or (automated) ribosomal intergenic spacer analysis (RISA and ARISA).
Effect of C/T −13910 cis-acting regulatory variant on expression …
2011年10月9日 · C/T − 13910 cis-acting regulatory variant located ≈ 14 kb upstream of lactase gene (LCT) completely correlates with lactase phenotype in Indian children. The genetic testing for the C/T − 13910 variant may be helpful in the diagnosis of adult-type hypolactasia in …
Real-time PCR based detection of the lactase non-persistence
2019年2月21日 · Primary hypolactasia is the main cause of lactose intolerance in adults. It is strongly associated with the single genetic variant LCT-13910C>T, located upstream of the lactase encoding gene. Consequently, analysis of LCT-13910C>T has been recommended as a direct genetic test for the trait.
deste trabalho foi estudar a diversidade do gene LCT, da região codificadora do gene, da região promotora proximal e da região enhancer população brasileira. Um total de 1297 indivíduos foram analisados.
Genotyping of the lactase-phlorizin hydrolase c/t-13910 …
The authors validate a denaturing high-performance liquid chromatography (dHPLC)-based assay versus conventional genotype sequencing in detecting the C/T(-13910) polymorphism of LCT and evaluate its prevalence in 2 different Italian geographical areas and in colorectal cancer patients.
- 某些结果已被删除