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Monogenic Obesity Genes Analysis
Genes tested (41)：
ADCY3, ALMS1, ARL6, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, CEP19, CEP290, CPE, CUL4B, DYRK1B, GNAS, KSR2, LEP, LEPR, MAGEL2, MC3R, MC4R, MKKS, MKS1, NR0B2, NTRK2, PCSK1, PHF6, PHIP, POMC, PPARG, SDCCAG8, SH2B1, SIM1, TRIM32, TTC8, TUB, UCP3, VPS13B, WDPCP.
Test details:
The Monogenic Obesity Genes Analysis offers an in-depth genetic evaluation targeting 41 genes associated with monogenic obesity. This advanced screening is crucial for diagnosing and guiding the management of patients who may have obesity due to single-gene mutations. By analyzing both coding and non-coding DNA regions, the test presents a thorough assessment of genetic factors contributing to obesity.
Although highly effective in detecting a spectrum of genetic variants, from single nucleotide polymorphisms to insertions, deletions, and copy number variations, the test may not identify certain complex genetic rearrangements. It accepts diverse sample types, ensuring optimal DNA quality for analysis.
This comprehensive the test results include an extensive interpretation of the genetic variants discovered, which is instrumental for healthcare providers in making informed decisions about patient care. This analysis is particularly insightful for confirming analysis dominant genetic disorders and identifying heterozygosity in recessive conditions.
In summary, the Monogenic Obesity Genes Analysis is an indispensable genetic testing tool that significantly enhances our understanding and management of monogenic obesity.