Protein sy'n cael ei godio yn y corff dynol gan y genyn FSHR yw FSHR a elwir hefyd yn Follicle stimulating hormone receptor (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 2, band 2p16.3.[2]
Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn FSHR.
- "A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency. ". Fertil Steril. 2017. PMID 29157895.
- "[Study of two Chinese families affected with resistant ovarian syndrome resulted from novel mutations of FSHR gene]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID 28397217.
- "Functional characterization of two naturally occurring mutations V221G and T449N in the follicle stimulating hormone receptor. ". Mol Cell Endocrinol. 2017. PMID 27889471.
- "The carriers of the A/G-G/G allelic combination of the c.2039 A>G and c.-29 G>A FSH receptor polymorphisms retrieve the highest number of oocytes in IVF/ICSI cycles. ". J Assist Reprod Genet. 2017. PMID 27817039.
- "Association of a promoter polymorphism in FSHR with ovarian reserve and response to ovarian stimulation in women undergoing assisted reproductive treatment.". Reprod Biomed Online. 2016. PMID 27448492.