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Rodinia – Female Infertility Panel (55 genes)

Known as: Rodinia Female Infertility panel 55 genes
SKU: GEN-ROD001MG

2,670.00

Research material: buccal mucosa smear
Response time (working day): 25
The test is done on an empty stomach: no
Home call service: Yes
Country: EU

General Information

Sampling for research will be done:

  • In the regions: Thursday   
  • In Tbilisi: Thursday and/or Friday (first half of the day)

Samples will be sent on Friday afternoon! For this, the sample must be sent to the central laboratory by Friday 12:00.

For interpreting research results Laboratory ""Synevo" We offer MEDICOVER Genetics  Geneticist's free Consultation

What is Rodinia?

Rodinia is a study that provides screening for genetic mutations associated with infertility.

Infertility is a major pathology of the reproductive system in which conception and maintenance of pregnancy are difficult or impossible.

Worldwide, 6 in every 1 couples experience infertility. 35% of infertility cases are due to male infertility, and 45% to female infertility. The remaining cases are the result of a combination of both causes.

Infertility has many different causes, including genetic ones. Laboratory studies, ultrasound imaging, and sperm analysis reveal 65% of infertility cases. Genetic causes of infertility are observed in 10-15% of men and women.

Genetic tests for infertility investigate these causes, allowing for informed decision-making and optimal clinical management of the condition.

 

The Rodinia – Female Infertility Panel tests for single nucleotide variants, insertions and deletions, and copy number variants in genes associated with female infertility. The panel also detects complete, partial, and mosaic changes in sex chromosomes.

 How many genes does the Rodinia female infertility panel test for?

The Rodinia Female Infertility Panel tests for 55 genes as well as X chromosome aneuploidies.

 

Study sample: Cheek swab

genes

AIRE, ANOS1, BMP15, CAPN10, CHD7, CYP11A1, CYP17A1, CYP19A1, DENND1A, DUSP6, EIF2B2, EIF2B3, FEZF1, FGF8, FGF17, FGFR1, FIGLA, FLRT3, FMR1, FOXL2, FSHB, FSHR, GALT, GDF9, GNAS, GNRH1, GNRHR. HESX1, HS6ST1, IL17RD, INS, INSR, IRS1, IRS2, KISS1, KISS1R, LHB, LHCGR, NOBOX, NR5A1, NSMF, POF1B, POLG, PROK2, PROKR2, PSMC3IP, SEMA3A, SPRY4, STAG3, TAC3, TACR3, THADA, WDR11, WT1, ZP1

When should we take the test?

Who is Rodinia intended for?

  • For individuals with fertility problems
  • For individuals with a specific phenotype who have a genetic syndrome associated with sex chromosome aneuploidy
  • During irregular or absent cycles
  • For people in need of assisted reproductive treatment
  • For oocyte (egg) donors
  • For individuals with a family history of infertility

Possible interpretation of the results

What diseases are associated with the genes examined by this panel?

  • Primary ovarian insufficiency
  • Polycystic ovary syndrome
  • Ovarian hyperstimulation syndrome
  • Hypogonadotropic hypogonadal disorders, such as Kallmann syndrome
  • Disorders of sexual development

Reference values

Important information

  • The buccal mucosa sample should be collected immediately after opening the package.
  • 60 minutes before sample collection, the patient is prohibited from: smoking, taking food and liquids (except water), brushing teeth and chewing gum
  • Please follow the instructions for specimen labelling, collection and transport carefully.
  • Check that all patient identification data is correct and compliant before specimen packaging and shipping

 

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This medical information is not intended to be a universal treatment guide for all patients. The treatment process, including the type, volume, and frequency of diagnostic tests and therapeutic procedures, is determined by the physician individually — based on an assessment of the patient's condition and relevant medical indications. The decision is made in consultation with the patient. Before purchasing a test, please read the instructions for its preparation.
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